Ali Zuweid’s Political Programme · Proposed bill · Health, Social Protection and Family
Public Health and Modern National Health System Law
A proposed federal law repealing and replacing the general framework of Public Health Law No. (89) of 1981, as amended. It connects the right to health with system governance, primary healthcare, surveillance, emergencies, workforce, data and accountability, respecting constitutional responsibilities and retaining separate specialist regulation of health insurance, medicines, patients’ rights and data protection.
Executive summary
Iraq’s general federal public-health framework still rests on Law No. (89) of 1981, as amended. Despite repeated updates, including legislation in 2021 and a 2026 decision raising a penalty, its original structure predates the 2005 Constitution, digital transformation, COVID-19, modern health insurance and new health-security capacity assessments. This file therefore proposes repeal and replacement legislation rather than another partial amendment.
The draft preserves matters belonging in specialist laws: Health Insurance Law No. (22) of 2020 and judicial modifications, patients’ rights and medical liability, mental health, medicines, food and medical devices, and data protection. It instead establishes a national public-health and system framework defining core functions, planning responsibilities, service packages, primary care, referral, workforce, surveillance, emergencies, information, contracting and oversight.
It draws on constitutional Articles (30), (31), (114/Fifth), (115) and (121). Because general health policy is shared, the Law is framed as federal coordination and national minima for functions requiring Iraq-wide links, expressly preventing interpretations removing regional powers or regional-law priority in conflicting shared matters.
It also draws on current reforms: expanding health insurance, HeRAMS monitoring of resources and services, the National Strategy for Women’s, Children’s and Adolescents’ Health 2025–2030, the Antimicrobial Resistance Plan 2026–2030 and the Joint External Evaluation of International Health Regulations capacities published in 2025. The proposed result is implementable legislation, not a hospital-building plan or separate financing programme.
Constitutional and legal context
Constitutional right to health
Article (31) guarantees every Iraqi healthcare and obliges the state to protect public health and provide prevention and treatment. Article (30) establishes health and social security. Article (114/Fifth) makes general health policy a shared responsibility of federal, regional and non-regional governorate authorities, while Articles (115) and (121) address regional-law priority and non-exclusive powers.
Existing law
Public Health Law No. (89) of 1981 remains effective as amended. It covers extensive preventive, treatment, laboratory and regulatory functions but belongs to an earlier constitutional and administrative framework. Partial updating continued through Amendment No. (20) of 2021 and a May 2026 Iraqi Gazette decision raising the Article (96/First/A) fine to one million dinars. Such targeted changes confirm continued operation but do not modernise the overall structure.
Health insurance as a separate legislative pathway
Health Insurance Law No. (22) of 2020 entered implementation, after which the Federal Supreme Court in case 60/Federal/2022 found several provisions unconstitutional. POL-72 therefore does not redesign insurance, contributions or its fund, but defines the service network and public-health functions with which insurance must integrate, avoiding duplicated institutions and conflicting financing.
Health-system transformation after 2020
Recent official sources show expanded measurement, coverage and reform. The Ministry of Health and WHO reported insured populations growing from 300 thousand in 2023 to 776 thousand in 2024. HeRAMS covers 5106 health-service delivery units as of 14 November 2024. Modern legislation therefore needs data, planning, purchasing, referral and integration rules, not merely traditional health functions.
Legislative choice
| Option | Assessment | Conclusion |
|---|---|---|
| Retain the 1981 Law with scattered amendments | Preserves a pre-constitutional structure and increases fragmented transitional provisions. | Not preferred. |
| Enact parallel legislation without repealing the old law | Duplicates powers, licences, penalties and cross-references. | Rejected. |
| Comprehensive repeal and replacement for public health and the health system | Unifies the general framework while preserving specialist laws and temporarily continuing regulations. | Selected option. |
Text of the draft Law
In the name of the people
Presidency of the Republic
Pursuant to enactment by the Council of Representatives and ratification by the President under Article (61/First) and Article (73/Third) of the Constitution of the Republic of Iraq of 2005, the following Law is issued:
Public Health and Modern National Health System Law
Part One — General provisions and definitions
Article (1) — Definitions
For this Law, unless context indicates otherwise, the following terms mean:
- Ministry: The federal Ministry of Health.
- Minister: The federal Minister of Health.
- Public health: Organised measures protecting and promoting population health, preventing disease, injury and disability, and responding to health risks through evidence and respect for rights and freedoms.
- National health system: Public, private and community institutions, resources, rules and programmes contributing to prevention, treatment, rehabilitation, palliative care and public health.
- Primary healthcare: Community-based care integrating health promotion, prevention, diagnosis, basic treatment, follow-up, referral, rehabilitation and palliative care according to need.
- Essential health services package: Priority preventive, treatment, rehabilitation and palliative services approved by the Ministry according to disease burden, clinical effectiveness, equity and available resources.
- Health facility: Any licensed public, private or community institution providing health, diagnostic, treatment, rehabilitation or prevention services.
- Local health authority: The health directorate or competent governorate health body under existing legislation.
- Referral: Documented transfer of care responsibility or requests for opinions or services between care levels.
- Health surveillance: Continuous systematic collection, analysis, interpretation and decision-making use of health data.
- Health event: An occurrence or group of occurrences potentially threatening public health.
- Disease outbreak: Disease, syndrome or pathogen incidence above expected levels in time, place or a defined population.
- Public-health emergency: A serious health event requiring exceptional, rapid coordination to protect people; not a constitutional state of emergency.
- One Health approach: Coordination of human, animal, environmental and food health against shared risks.
- National health information system: A standardised system collecting, linking, analysing and providing data for management, planning, surveillance and research with privacy protected.
- Underserved area: An area demonstrably deficient under published criteria in access, staffing, equipment, response time or service continuity.
Article (2) — Objectives
This Law modernises public-health legislation, governs the health system through the constitutional right to care, consolidates primary healthcare and tiered referral, promotes geographic equity, quality, safety and prevention, builds national surveillance and emergency response, improves workforce, resource, infrastructure and information planning, integrates public and private provision, and ensures transparency, accountability and sustainability.
Article (3) — Governing principles
- Rights to health and healthcare, with non-discriminatory access.
- Priority for prevention, primary care and early intervention, with specialist care integrated into the system.
- Equitable resource distribution according to population, disease burden, need, distance and vulnerability, not merely formally equal administrative allocation.
- Patient safety, care quality and evidence-based practice.
- Professional independence within standards and existing laws.
- Transparency, reviewable decisions and no immunity of administrative decisions from judicial challenge.
- Privacy, confidentiality and minimum necessary data collection.
- Community participation and intersectoral coordination.
- Fiscal and operational sustainability, linking expansion to staffing, operation and maintenance capacity.
- All-hazards preparedness and essential-service continuity during crises.
Article (4) — Scope and legislative boundaries
This Law applies to federal bodies, health authorities in governorates outside regions and public facilities, and to private and community facilities regarding licensing, reporting, surveillance, safety, public health and shared national obligations. It complements rather than replaces specialist insurance, patients’ rights, medical liability, mental-health, medicine, food, device, drug, environmental and data-protection legislation as the overarching system and public-health law.
Article (5) — Federal-system application
General health policy shall be developed cooperatively under the Constitution. This Law applies in the Kurdistan Region and other regions within federal powers or joint arrangements, respecting regional-law priority in conflicting shared matters. Regular technical, epidemiological and information-sharing mechanisms shall connect all parts of Iraq without changing constitutional responsibilities.
Article (6) — National minimum public-health protection
The Ministry, regions and governorates shall establish national reference standards for epidemiological surveillance, event reporting, laboratory safety, emergency response, immunisation, infection prevention and protective information exchange. These coordinate national action without creating constitutionally unrecognised exclusive federal powers.
Part Two — Policy, governance and planning
Article (7) — National health policy
The Ministry shall develop a four- to six-year national policy with federal bodies, regions, governorates, universities, professional associations, private providers and civil society. It shall specify priorities, outcomes, resource allocation, service mapping, workforce, digital transformation and emergency preparedness, published with financial summaries and clear indicators.
Article (8) — Health Policy Coordination Council
The Council of Ministers shall establish a coordinating council chaired by the Minister of Health with senior relevant, regional and governorate representatives, without replacing ministries or local authorities. It shall align policy, resolve intersectoral operational conflicts, review national risks, coordinate workforce, emergency and One Health plans, and publicly report annually to government and Parliament.
Article (9) — Needs-based planning
Planning shall use population, disease, mortality, disability, poverty, distance, travel time and actual facility capacity, plus use, waiting, referral and staffing data. Building or registered-bed counts alone must not imply capacity where facilities lack operation, equipment or staff. The Ministry shall publish and periodically update a unified service-gap methodology.
Article (10) — Essential health services package
Within twelve months of commencement, the Ministry shall approve a national package, reviewed at least biennially, covering prevention, immunisation, primary and emergency care, priority clinical services, maternity, children, chronic disease, rehabilitation and palliative care, with delivery levels and referral criteria. It shall not determine financing or cost-sharing governed by insurance and health-financing laws.
Article (11) — Service maps and geographic coverage
Local authorities shall annually map facility locations, opening hours, operational capacities, critical shortages, access times and rural and remote areas. Maps shall form an analysable national register with aggregate publication, informing investment, distribution and contracting.
Article (12) — Community participation and accountability
The Ministry and local authorities shall regularly hear patients, communities and providers and publish plans, results and performance summaries. Advisory councils may support major facilities or primary-care networks without independent executive or financial authority unless another law provides it.
Part Three — Service delivery and referral
Article (13) — Primary healthcare as the foundation
Primary care shall anchor prevention, immunisation, family, maternal and child health, chronic-disease follow-up, basic mental healthcare, education, early detection, basic treatment and referral. The Ministry shall develop centres from limited consultation units into continuing-care teams for defined service populations.
Article (14) — Family medicine and continuity
A phased national family-medicine and continuing-care programme shall include voluntary or existing insurance/service-based registration, multidisciplinary teams, chronic-disease follow-up and clear referral links. Lack of registration or an unobtainable referral document must not deny emergency or necessary services.
Article (15) — Referral system
A unified referral and back-referral system shall define conditions managed at each level, prioritisation, appointments and feedback. Facilities shall have reliable platforms or communications for available capacity and minimum necessary clinical summaries. Referral must not delay emergencies threatening life, organs or function.
Article (16) — Underserved-area services
Authorities shall provide tailored interventions where needed: longer opening hours, mobile teams, telemedicine, patient transport, regulated contracting and workforce incentives. Interventions require published gap measurements and annual outcome evaluation.
Article (17) — Emergency and pre-hospital services
The Ministry and relevant bodies shall organise integrated emergency medicine, ambulance and urgent referral, including triage, dispatch centres, ambulance and equipment standards, facility-capacity exchange and inter-hospital transfer protocols. Response indicators shall reflect urban and rural settings rather than one unrealistic national figure.
Article (18) — Specialist care and referral hospitals
Hospitals and specialist centres shall be classified by actual capacity and scope, with regional and national networks for complex services. New public hospitals or expansions require demonstrated population need, operating, staffing, maintenance and recurrent funding plans, and assessment of existing-network effects.
Article (19) — Rehabilitation and palliative care
Rehabilitation and palliative services shall enter essential packages and referral networks in hospitals, primary care and homes as needed. Standards shall prevent referral delay and maintain medicines, assistive devices and rehabilitation under specialist laws.
Part Four — Health workforce
Article (20) — Health workforce planning
A national workforce observatory shall maintain a unified register of specialties, locations, work patterns, vacancies and expected retirements, reporting annual gaps by governorate, specialty and care level. Admissions, training, recruitment and deployment shall reflect actual needs, coordinated with higher education, finance, service councils and professional bodies.
Article (21) — Equitable distribution and incentives
Published, time-limited financial, professional, housing, education and transport incentives may support underserved locations or scarce specialties. They shall be periodically evaluated for recruitment and retention effects, not substitute for safe, equipped and well-managed workplaces.
Article (22) — Continuing professional education
Health authorities shall require minimum continuing education appropriate to profession and risk, linking critical practice to demonstrated skills and regular training. Coordination with boards, associations and universities shall prevent conflicting or duplicate accreditation and support simulation in emergencies, resuscitation and infection control where needed.
Article (23) — Worker safety and protection
Facilities shall provide safe workplaces, protective equipment, infection prevention, occupational, radiation and chemical risk management, and assault and incident reporting. Good-faith reports of serious dangers or shortages threatening patients or workers must not be punished under existing legal protections.
Article (24) — Retaining and using expertise
The Ministry shall retain critical specialists and lawfully engage overseas Iraqi experts, retirees and private practitioners through training, part-time contracts or advice. Programmes must not bypass appointment rules, create conflicts or drain public capacity into unregulated private practice.
Part Five — Surveillance, prevention and disease control
Article (25) — National health surveillance
An integrated epidemiological and health surveillance system shall cover communicable and non-communicable diseases, antimicrobial resistance, significant deaths and unusual events, using standard case definitions, reference laboratories and electronic or outage-resilient alternative reporting. Actionable alerts must reach competent bodies without awaiting periodic statistical completion.
Article (26) — Notifiable diseases
The Minister shall issue and risk-update schedules of notifiable diseases, syndromes and events with urgency levels. Doctors, laboratories, facilities and relevant veterinary or environmental bodies shall report under prescribed rules, protecting identities and limiting use to public health, care, lawful research and judicial purposes where applicable.
Article (27) — Epidemiological investigation and contact tracing
For suspected significant infectious events, authorities may investigate, sample and trace contacts as necessary and proportionate. Instructions shall define access and retention periods. Public disclosure of affected or exposed persons’ names requires consent, a court order or exceptional statutory health necessity.
Article (28) — Isolation and quarantine
Isolation or quarantine requires a reasoned health-authority decision based on individual or collective risk and scientific criteria, for the shortest necessary period, with humane conditions, care and communications. Persons shall be informed of reasons, duration and rights, including urgent judicial challenge. Collective measures require periodic review and must not be punitive.
Article (29) — Mandatory testing and prevention
A specified examination or preventive measure may be required only for a serious, established threat where no less restrictive effective alternative exists, respecting medical contraindications, privacy and dignity. Compulsory treatment solely for public benefit requires express statutory authority and strict judicial and medical safeguards.
Article (30) — National immunisation
The Ministry shall adopt an evidence-based schedule, ensure essential vaccines and monitor safety and cold chains, publishing aggregate coverage and adverse events. Specific vaccination requirements for high-risk occupations, settings or outbreaks require legislation or clearly delegated instructions, with medical exceptions and reasonable alternatives.
Article (31) — Reference laboratories and diagnostic networks
The Ministry shall organise public-health reference laboratories and standards for quality, biosafety, sample referral, reference confirmation and genomic testing where needed. Public and private laboratories conducting public-health-significant tests must report, meet quality requirements and participate in external proficiency testing.
Article (32) — Facility infection control
Every facility shall maintain effective infection prevention and control with clear responsibilities, healthcare-associated infection surveillance, hand hygiene, sterilisation, sharps and medical-waste management coordinated with environmental bodies, and outbreak plans. The Ministry shall publish aggregate indicators and support improvement rather than punishment alone.
Article (33) — Antimicrobial resistance
The state shall adopt One Health against antimicrobial resistance. Health, Agriculture, Environment, Higher Education and regulators shall establish surveillance, stewardship, laboratory, research and awareness programmes. Hospitals require stewardship programmes; resistance data must not justify withholding necessary treatment.
Part Six — Health emergencies and health security
Article (34) — Health risks and emergencies
Periodic national assessment shall cover epidemic, chemical, radiological and environmental hazards, disasters, mass casualties and supply-chain disruption. It shall inform a multi-hazard preparedness and response plan linked to national crisis management and civil defence and tested through regular exercises.
Article (35) — Declaring public-health emergencies
On the Minister’s reasoned recommendation, the Council of Ministers may declare a geographically and temporally defined emergency where a widespread event threatens system capacity or population safety. The immediately published decision shall define area, duration, measures and responsible bodies. It does not replace constitutional emergency procedures or permit suspension of the Constitution or rights beyond lawful limits.
Article (36) — Emergency response powers
Within the declaration, temporary measures may redistribute health resources, mobilise stocks, operate alternative facilities, extend hours, manage referrals, assign response teams, impose temporary health conditions on gatherings or activities and activate statutory public-health orders. Measures shall be necessary, proportionate, time-limited and reviewable.
Article (37) — Essential-service continuity
Health directorates, referral hospitals and primary-care centres shall plan crisis continuity for electricity, water, oxygen, communications, medicines, fuel, operational alternatives, supplies and staff, testing regularly and updating after major incidents.
Article (38) — Strategic medical stocks
National or distributed strategic stocks for epidemics and disasters shall reflect risks and expiry cycles preventing spoilage. Digital or auditable records, stock rotation and periodic independent review are required. Emergencies justify direct procurement only within statutory exceptions and with subsequent documentation.
Article (39) — National International Health Regulations authority
The Council of Ministers, on the Ministry’s proposal, shall designate the authority coordinating applicable International Health Regulations and define links to the national focal point, border crossings and ministries. It shall coordinate, monitor, assess capacities and report under Iraq’s obligations without granting international organisations direct authority over domestic sovereign decisions.
Article (40) — Border crossings and international transport
Health, border, transport, interior, agriculture and environment authorities shall provide core capacities at designated crossings, detection, response, case transfer and laboratory links, protecting health with minimum unnecessary disruption of travel and trade. Travel restrictions require periodic risk-based review.
Part Seven — Population health and multisectoral prevention
Article (41) — Maternal, child and adolescent health
National policy shall ensure continuous maternal, newborn, child and adolescent care before pregnancy, through pregnancy, birth and afterwards, including nutrition, immunisation, early detection, school health and age-appropriate services. It shall respect the approved national strategy and review outcomes by governorate and groups most exposed to deprivation.
Article (42) — School and university health
Health and education ministries shall organise immunisation, periodic examinations, basic mental healthcare, education, nutrition, healthy environments and infectious-disease response. School screening must not stigmatise or exclude students except under temporary lawful health necessity with suitable alternatives.
Article (43) — Nutrition and community health
Authorities shall monitor malnutrition, obesity and nutrient deficiencies, promote healthy diets and improve public-institution and school food environments. Mandatory food safety, labelling and product rules remain under specialist law, with the Ministry advising on health risks and technical recommendations.
Article (44) — Non-communicable diseases
Primary care shall integrate prevention, early detection and ongoing cardiovascular, diabetes, cancer, chronic respiratory and other disease management, with clear referrals and evidence-based tests. Multisectoral policies shall reduce risk factors consistently with specialist tobacco, food, environmental and traffic laws.
Article (45) — Occupational health
Health, Labour and oversight bodies shall develop occupational disease and injury surveillance, aggregate data exchange and examination and prevention guidance for high-exposure groups. Employer responsibilities, compensation, insurance and safety remain governed by labour, social security and specialist laws.
Article (46) — Environmental and climate health
The Ministry shall assess environmental and climate health impacts, monitor indicators associated with heat, air and water pollution and hazardous substances, and issue warnings and technical advice. This does not diminish Environment Ministry, local or specialist statutory powers.
Article (47) — Injury and accident prevention
The Ministry and competent bodies shall monitor injuries from traffic, violence, burns, falls, drowning and other causes, using data for prevention and better emergency care. Injury prevention belongs in health policy without making the Ministry a traffic, security or municipal enforcement agency.
Part Eight — Information, digitalisation and research
Article (48) — National health information system
National information architecture shall define standards, terminology, core datasets, interoperability, quality checks and reporting frequency. Publicly funded facilities and private providers contracted by government or subject to surveillance shall supply minimum prescribed data lawfully.
Article (49) — Electronic health records and interoperability
Electronic records shall be phased in with referral, laboratory, medicine and appointment systems using reliable identifiers and national interoperability standards. One central database is not required where a federated or distributed architecture provides safer, more efficient exchange.
Article (50) — Data protection and confidentiality
Health-data processing shall be necessary, proportionate and purpose-limited, applying minimisation, access controls, encryption, audit and logs. Detailed rights follow specialist data-protection law. Epidemiological reporting does not authorise identifiable publication or sharing beyond legitimate health need.
Article (51) — Data quality and audit
The Ministry shall define indicators, completeness and consistency tests, sample audits, corrections and prevention of manipulation incentives. Provisional and final data must be distinguished and reference years and methodologies disclosed.
Article (52) — Open data and transparency
The Ministry shall regularly publish aggregated, anonymised health data on resources, services, diseases, indicators, expenditure, waiting times and quality, in reusable formats where possible, taking account of security, privacy and small statistical cells that may identify individuals. A special regulation shall specify legitimate exceptions and publication schedules.
Article (53) — Health research and use of evidence
The State shall encourage applied health research and policy evaluation and ensure the independence of research ethics committees and participant safety. The Ministry shall use economic and health assessments, systematic reviews and local data to set priorities; cost alone must not be used to deny a group a necessary intervention in a discriminatory manner.
Article (54) — Health technology assessment
The Ministry shall establish an institutional health technology assessment function covering medicines, devices, procedures and digital programmes in terms of effectiveness, safety, value and suitability for the system. Assessment findings shall inform the essential package, procurement and contracting, in coordination with the competent medicines and devices regulator when established, or under legislation in force.
Part Nine — The private sector, regulation and inspection
Article (55) — Public–private sector integration
The private sector shall be treated as a regulated partner in the health system, rather than a substitute for State responsibility. The Ministry shall set data-sharing, surveillance, referral, emergency, contracting and quality requirements for private facilities, publish contracting rules and prevent conflicts of interest. No privileges or exclusive referrals that violate competition or harm a public facility may be granted without publicly stated justification.
Article (56) — Purchasing services and contracting
Public bodies may purchase health services from private or non-governmental providers where need and contracting and oversight capacity are demonstrated, using quantitative and qualitative indicators, clear payment mechanisms and audit. Contracts shall be subject to the procurement and contracts law in force. Payment for undocumented services and incentives encouraging excessive medical procedures are prohibited.
Article (57) — Health licensing and inspection
No health facility or activity subject to health oversight may operate without a licence under the law. Inspection shall be risk-based, using publicly available checklists wherever possible. Inspectors shall produce a reasoned record documenting the violation and evidence and give the establishment a proportionate correction period, except where imminent danger permits immediate temporary closure.
Article (58) — Temporary closure and corrective measures
The health authority may suspend a specific service or part of a facility, or temporarily close the facility, where a direct, serious health risk is established and cannot be contained by a less restrictive measure. The decision must be written, reasoned and time-limited, specify reopening conditions, and ensure continuity of patient care and safe transfer. It shall be subject to administrative grievance and judicial appeal.
Article (59) — Preventing conflicts of interest
Staff, committees and experts involved in licensing, contracting, standard-setting and technology assessment shall disclose relevant financial and professional interests and refrain from participating where a material conflict exists. The Ministry shall publish a unified conflicts-of-interest policy and a register of disclosures for committees whose work affects the public, insofar as privacy is respected.
Part Ten — Financing, investment and sustainability
Article (60) — Public health financing
The general budget shall allocate sufficient resources to essential public health functions that cannot rely on individual payments, including surveillance, laboratories, immunisation, emergency response, school health, prevention and data. Each year, the Ministry shall state the estimated cost of these functions, the financing gap and its effect on preparedness.
Article (61) — Linking facility budgets to activity and need
The Ministries of Health and Finance shall progressively develop financing methods linking part of facility budgets to population need, activity volume and type, quality and geographical deprivation, while protecting essential small facilities in remote areas. Activity-based payment must not be applied in a way that encourages unnecessary services or neglect of prevention.
Article (62) — Maintenance and asset life cycles
Health equipment and infrastructure projects shall not be approved without a life-cycle plan covering operation, maintenance, spare parts, training, depreciation, energy and replacement. Facilities shall allocate a clear budget line or percentage to preventive maintenance and document critical equipment failures and repair times. Procurement of equipment without reasonable operating and maintenance capacity is prohibited.
Article (63) — National health accounts and expenditure
In cooperation with statistical and financial bodies, the Ministry shall prepare periodic national health accounts using a recognised methodology, identifying funding sources, payers, service providers and expenditure categories. Results shall be published with data limitations disclosed and used to monitor financial protection and allocative efficiency, without conflating them with Health Insurance Fund data.
Article (64) — Protecting public health investment
Major health projects shall undergo prior assessment of need, feasibility and operation, followed by review of whether results were achieved. A stalled or unjustified project may be reprogrammed where evaluation establishes that completion would yield less benefit than an alternative, while protecting public funds and contractual obligations under the law.
Part Eleven — Performance and accountability
Article (65) — National performance indicators
The Ministry shall adopt a limited and relatively stable set of national performance indicators covering access, coverage, waiting times, referral, geographical equity, workforce, care safety, continuity of medicines and services, emergency preparedness and data quality. It shall publish each indicator’s definition, source and update frequency. Definitions may not be changed without explaining the effect on comparability over time.
Article (66) — Annual national health report
During the first half of each year, the Minister shall issue a report on the preceding year covering public health status, policy implementation, service gaps, primary care and hospital performance, workforce, surveillance and emergencies, expenditure, data and disparities between governorates, and action taken to address shortcomings. The report shall be sent to the Council of Ministers and Council of Representatives and published for the public.
Article (67) — Independent evaluation
Every four years, national health system performance and implementation of this Law shall undergo independent evaluation by an academic or oversight body or consortium of experts operating under safeguards for independence and conflicts of interest. Evaluation shall cover health outcomes, equity, efficiency, preparedness, data quality and the impact of regulatory measures. Its summary, the Ministry’s response and the remedial plan shall be published.
Article (68) — Complaints and grievances
Each health body shall maintain a clear mechanism for receiving complaints and grievances concerning services, administrative decisions, inspection and oversight, with response deadlines and an escalation route. These mechanisms shall not prejudice an affected person’s right to seek judicial or oversight review or claim compensation under the law.
Article (69) — Protecting those reporting public health risks
No retaliatory employment or contractual action may be taken against anyone who reports in good faith manipulation of surveillance data, a serious risk, concealment of an outbreak or corruption in health procurement. The protection provisions of legislation in force shall apply. Protection shall not extend to malicious reports or unlawful disclosure of patient data.
Part Twelve — Sanctions and safeguards
Article (70) — Administrative violations
Without prejudice to any harsher penalty under another law, administrative violations include failure to submit mandatory data after warning, obstruction of inspection, breaches of licensing conditions that do not directly threaten life, and failure to implement a binding corrective plan. A warning, administrative fine, service suspension or licence suspension may be imposed according to severity and repetition. Schedules and financial limits must be set by law or regulation based on express legislative delegation; penalties must not be discretionary without an upper limit.
Article (71) — Offences relating to public health
Anyone who intentionally falsifies or conceals material outbreak data, deliberately obstructs implementation of an enforceable judicial or administrative health order so as to expose the public to serious danger, or deliberately destroys surveillance samples or evidence connected with an official investigation shall be punished under the Penal Code or special laws. Criminal liability shall not arise from mere professional error or good-faith scientific disagreement unless expressly criminalised by law.
Article (72) — Enforcement and inspection safeguards
Inspection shall remain within the inspector’s competence, with official identification shown and procedures documented. A private dwelling or place not open to the public shall not be entered without its owner’s consent or a judicial warrant, except where imminent danger legally permits and requires immediate intervention. Health record confidentiality shall be respected. Originals shall not be seized except where necessary and under an official record, with a copy provided to the facility where possible.
Article (73) — Administrative grievance and judicial appeal
An administrative decision issued under this Law may be challenged before the superior authority within the periods specified by instructions, without prejudice to the right of appeal to the competent court. No subordinate provision may render a committee, ministerial or health department decision final or immune from judicial review contrary to the Constitution.
Article (74) — Compensation and liability
Application of public health orders shall not prejudice an affected person’s right to seek compensation for unlawful fault, negligence or abuse of authority under general rules. Compensation from the State shall not arise merely from implementation of a lawful measure, unless the law provides otherwise or an implementation error causes disproportionate harm.
Part Thirteen — Final and transitional provisions
Article (75) — Regulations and instructions
The Council of Ministers and Minister, each within their competence, shall issue the regulations and instructions necessary to implement this Law within one hundred and eighty days of its publication, particularly concerning the service package, surveillance, reporting, health emergencies, isolation and quarantine, laboratories, referral, the information system, inspection and performance indicators. Instructions affecting the public shall be published in the Iraqi Gazette or another legally authorised medium.
Article (76) — Review of existing health legislation
Within twelve months, the Ministry of Health, in coordination with the State Council and competent bodies, shall prepare a schedule of legislation, regulations and instructions requiring amendment, repeal or consolidation as a result of this Law taking effect. Priority shall be given to old provisions inconsistent with the Constitution, institutional or technological developments, or judicial review principles.
Article (77) — Retention of specialist legislation
Laws governing insurance and health insurance, health professions, tobacco, narcotics, medicines, food and medical devices, the environment, labour, forensic medicine and other special health legislation shall remain in force unless inconsistent with an express provision of this Law or duly amended. This Law shall not be interpreted as transferring the competence of an existing authority or institution without express provision.
Article (78) — Repeal of Public Health Law No. 89 of 1981
Public Health Law No. (89) of 1981, as amended, shall be repealed when this Law takes effect, subject to the transitional provisions of Article (79). References in laws and regulations to the repealed law shall be treated as references to the corresponding provision of this Law insofar as the subject permits, pending legislative correction of those references.
Article (79) — Continuation of previous regulations, instructions and decisions
Regulations, instructions, notices and regulatory decisions issued under the repealed Public Health Law shall remain effective for no more than two years after this Law takes effect, insofar as they do not conflict with its provisions, until replaced or amended. The Ministry shall publish a public register identifying what remains in force and what has been repealed or replaced to avoid legal uncertainty.
Article (80) — Continuation of existing licences and rights
Health licences, permits and approvals valid when this Law takes effect shall continue until expiry unless a serious risk requires reconsideration, and shall be subject to the new requirements on renewal. A change in the legal regime shall not extinguish an acquired right or valid contractual obligation except under the law and requirements of public interest, with compensation where due.
Article (81) — Principal transitional deadlines
- Within three months: establish the Health Policy Coordination Council and designate the lead for implementation of the Law.
- Within six months: adopt surveillance and reporting definitions, the health emergency framework, inspection rules and a plan to replace old instructions.
- Within twelve months: adopt the essential services package, service-gap methodology, workforce plan and health information architecture.
- Within eighteen months: publish the first integrated national map of services and operational capacity, and the first report on gaps in underserved areas.
- Within twenty-four months: complete the public register of repealed or replaced instructions and connect most public facilities to a unified minimum dataset.
Article (82) — Entry into force
This Law shall enter into force one hundred and eighty days after publication in the Official Gazette, except provisions concerning issuance of regulations and instructions and preparatory work, which shall apply from publication. Public Health Law No. (89) of 1981, as amended, shall continue to apply during the transition until the repeal stipulated in Article (78) takes effect.
Statement of reasons
To implement the constitutional provisions guaranteeing the right to healthcare and health insurance and entrusting public authorities with public health; to modernise the legal framework still based on Public Health Law No. (89) of 1981, as amended, and align it with the federal constitutional order and developments in primary healthcare, health insurance, epidemiological surveillance, health emergencies, digital information and antimicrobial resistance; to allocate resources according to need and improve referral, workforce, maintenance and transparency; and to unify administrative and judicial safeguards in health oversight without creating unnecessary parallel bodies, this Law is enacted.
Explanatory memorandum
1. Why is replacement preferable to a ninth or tenth amendment?
The 1981 Law is broad and historically important, but predates the 2005 Constitution and today’s institutional and digital transformation. Partial amendments addressed individual matters without shifting the Law’s logic from a list of powers and oversight provisions to a modern governance system. Replacement allows its scope to be redefined, distinguishes it from health insurance, medicines and patient rights, and establishes an orderly legal transition instead of retaining multiple layers of provisions.
2. Relationship with the Health Insurance Law
Health insurance answers the question: who pays, and how are risks pooled and coverage managed? This Law answers: how are the health system, public health functions, network, referral, surveillance and preparedness organised? Separating these functions is essential. POL-72 establishes a reference services package and delivery pathways, while contributions, entitlements, cost-sharing rates, the Authority and Fund remain within POL-73 and the existing insurance law.
3. Why put primary care at the centre of the Law?
Sending every health problem to a hospital increases costs and waiting times and weakens prevention. The proposal therefore makes primary care the anchor, with organised referral and clear emergency exceptions. It does not impose a rigid mandatory spending share or predetermine the number of centres; it requires service gaps to be measured and mapped publicly and investment linked to need.
4. Health federalism
Health is not an exclusively federal competence. The proposal therefore avoids wording that would make the federal Ministry the direct manager of every facility in a region. Functions requiring national coordination—such as surveillance, response to cross-border events, data definitions, reference laboratories and certain emergency standards—are framed as coordination standards and shared reference frameworks. Where conflict arises over a shared competence, constitutional rules on the precedence of regional law shall be respected.
5. A health emergency is not a constitutional state of emergency
The proposal expressly distinguishes a temporary administrative health declaration from a constitutional state of emergency. A health emergency declaration allows resources to be mobilised, response plans activated and specific health measures prescribed by law imposed; it does not confer unlimited power, suspend the Constitution or eliminate judicial oversight. This distinction matters in preventing expansion of public health powers after the pandemic experience.
6. Isolation and quarantine with safeguards
Isolation and quarantine may be necessary for certain infectious diseases but restrict liberty. The proposal therefore requires a reasoned decision, necessity and proportionality, the shortest necessary duration, humane conditions and access to judicial appeal. It does not permit a health measure to become punishment or indefinite detention.
7. Digital data are not an end in themselves
The proposal does not mandate a vast central database. It requires interoperability standards and a minimum dataset, leaving the technical architecture centralised or distributed according to security and efficiency. This reduces vendor lock-in risks and preserves compatibility with future data protection and digital government legislation.
8. No arbitrary construction figures
The Law does not set a fixed number of hospitals, beds or ambulances, or a uniform physician ratio for all Iraq, because these decisions change with population, epidemiology and resources. Instead, it requires a national planning methodology, annual maps, actual operational capacity and life-cycle appraisal before investment. This makes the legislation durable rather than a frozen budget plan embedded in law.
9. Judicial oversight
The proposal avoids the model of older provisions that made some closure or committee decisions final or barred legal proceedings. Article (100) of the Constitution prohibits shielding any administrative act or decision from appeal. The Federal Supreme Court’s decision on the Health Insurance Law also demonstrated the importance of this rule. All administrative health decisions are therefore subject to judicial review.
10. Updating functions without creating a new bureaucracy
The proposal does not create a new independent national public health authority. Leadership remains with the Ministry of Health and existing health authorities, with only a coordination council established to address the shared nature of health policy. New functions—the observatory, technology assessment and data quality—can be established as units within the Ministry rather than separate legal entities, unless institutional independence is later shown to be necessary.
Alignment with existing legislation
| Area | Status | Treatment |
|---|---|---|
| Public Health Law No. 89 of 1981 | The existing general framework. | Repeal and replacement when the new Law takes effect, with instructions temporarily retained. |
| Ministry of Health Law No. 10 of 1983, as amended | Governs the Ministry’s structure and powers. | Remains in force; its organisational provisions should subsequently be reviewed to avoid duplicate definitions of councils and departments. |
| Health Insurance Law No. 22 of 2020 | Governs coverage, insurance and its institutions. | Remains a separate legislative track, integrated with the services package and network. |
| Patient rights and medical liability | Require comprehensive specialist regulation. | Does not pre-empt POL-74; limited to public health and administrative safeguards. |
| Medicines, food and medical devices | Regulated by scattered legislation and decisions. | Leaves detailed regulation to POL-75 and legislation in force. |
| Mental health | Requires a specialist rights-based framework. | Leaves details to POL-76 and covers only integration into primary care. |
| Personal data protection | A sensitive cross-cutting area. | Establishes minimum health principles, with priority for the Data Protection Law once enacted. |
| Environment and waste | Separate environmental competences. | Limits health’s role to impact assessment, surveillance and coordination. |
Implementation and transition requirements
Success depends on replacing old regulations gradually, rather than repealing them in a single day. The proposal therefore allows 180 days before entry into force and retains previous instructions for up to two years insofar as they do not conflict. It also requires a public register of effective and replaced regulations—an important tool, since reforming the 1981 Law risks creating a regulatory vacuum in licensing, inspection and laboratories if the underlying law is repealed without replacement regulations.
| Period | Regulatory or institutional output | Purpose |
|---|---|---|
| 0–3 months | Implementation leadership unit + coordination council + inventory of old regulations. | Prevent fragmented responsibility. |
| 0–6 months | Surveillance definitions, reporting rules, health emergency framework and inspection rules. | Protect functions that cannot tolerate a vacuum. |
| 6–12 months | Services package, service-gap map, workforce plan and referral standards. | Turn the Law into national operating rules. |
| 12–18 months | Health information architecture, minimum dataset and published service maps. | Data-informed decision-making. |
| Up to 24 months | Replace principal old regulations and publish the legal-status register. | Complete the transition. |
Financial and implementation impact
This Law is not a construction programme and does not justify an arbitrary total cost. Its direct financial impact arises chiefly from regulatory functions and capabilities that should already exist or can be developed within the Ministry: surveillance, data quality, service mapping, a workforce observatory, emergency stocks, referral standards and health technology assessment. Hospitals, equipment and network expansion remain subsequent budget and investment decisions conditional on needs and life-cycle analysis.
Before executive referral, a financial Regulatory Impact Assessment must be prepared, covering limited establishment costs for each new function, annual operating costs, existing resources that can be reused, information-system development costs, and costs of updating regulations and training. It must distinguish the Law’s regulatory expenditure from health-sector capital expenditure so that costs unavoidable in any event are not attributed to the legislation.
| Item | Required calculation method | Control |
|---|---|---|
| Surveillance and laboratories | Workforce, equipment and connectivity gaps for each governorate. | Avoid counting existing resources twice. |
| Health information | Cost standards, integration, security and training, without assuming procurement of a single central system. | Avoid vendor lock-in and unnecessary licences. |
| Workforce | Specialty and location gaps and targeted incentives. | Make incentives conditional on results. |
| Emergencies and stocks | Risk analysis + minimum days of coverage + stock rotation. | Prevent expiry and stockpiling. |
| Inspection and regulation | Inspector and visit numbers based on risk, rather than the raw facility count. | Risk-based oversight. |
Relevant international reference frameworks
The proposal does not transplant any single country’s model. It uses established health-system reform principles: primary healthcare as the foundation of universal health coverage; allocation by need and equity; purchaser–provider separation where appropriate without imposing one model; reliance on surveillance and data; all-hazards emergency management; and proportionality and judicial review of public health measures.
For health security, the proposal draws on the amended International Health Regulations generally effective since 19 September 2025, particularly the need for a national coordination authority, point-of-entry capacities, notification and preparedness. It also aligns with Iraq’s Joint External Evaluation published in 2025 and the updated 2026–2030 antimicrobial resistance plan based on One Health.
Sources and references
- Constitution of the Republic of Iraq, 2005 — Iraqi Council of RepresentativesThe constitutional basis for the right to healthcare and health insurance; Article 114/Fifth on formulating general health policy in cooperation with regions and governorates; and Articles 115 and 121 on allocation of competences.
- Ministry of Justice — Public Health Law No. (89) of 1981, as amendedThe official translated text published by the Iraqi Gazette Directorate; confirms that the 1981 Law remains the existing general framework with successive amendments.
- Ministry of Justice — Iraqi Gazette No. 4627Contains Law No. (20) of 2021 amending Public Health Law No. (89) of 1981.
- Ministry of Justice — Iraqi Gazette No. 4867, 18 May 2026Contains a decision amending the fine amount in Article 96/First/A of the Public Health Law, providing recent evidence that the old law remains in force with piecemeal adjustments.
- Health Insurance Law No. (22) of 2020 — Ministry of JusticeReference for separating health insurance regulation from this framework law.
- Federal Supreme Court — Decision 60/Federal/2022Declared several Health Insurance Law provisions unconstitutional, affirmed their relationship to Articles 30 and 31 of the Constitution, and stressed that administrative decisions must remain subject to constitutional and judicial oversight.
- WHO — HeRAMS Iraq: Operational status of the health system, November 2024A relatively recent assessment of resource and service availability, based on data from 5106 health service delivery units as of 14 November 2024.
- WHO/Ministry of Health — World Health Day 2025 statementDocuments progress in implementing the Health Insurance Law and increased coverage from 300 thousand people in 2023 to 776 thousand in 2024, supporting coordination of framework reform with the existing insurance system.
- WHO — Joint External Evaluation of IHR core capacities in Iraq, mission 17–21 September 2023, published 2025Reference for designing emergency preparedness and national public health capacity provisions.
- WHO — Amended International Health Regulations, generally effective since 19 September 2025Reference for international coordination, the national authority, points of entry, notification and health emergency preparedness.
- WHO/Ministry of Health — National Action Plan on Antimicrobial Resistance 2026–2030Reference for One Health, surveillance and antimicrobial stewardship.
- WHO — National Strategy for Women’s, Children’s and Adolescents’ Health 2025–2030Reference for integrating services across the life course, equity and access in underserved areas.
- WHO — Primary health careInternational reference for the central role of primary healthcare in universal health coverage and continuity of care.
- WHO — Universal health coverageReference for access to quality health services without financial hardship, while retaining insurance mechanisms in the specialist law.
- WHO — Evaluation of WHO contribution in Iraq: Executive summary, 2025Relatively recent institutional context for Iraq’s transition from humanitarian response to building sustainable health systems.
A proposed bill within Ali Zuweid’s political programme. Prepared by Ali Zuweid. Last updated: 5 October 2026.