Medicines and Allied Substances 2013 (No. 3 of 2013)
ZambiaAct of Parliament2013No. No. 3 of 2013
In force, and amended by 1 amendment Act. Check the amendments before relying on the wording of a section.
The Medicines and Allied Substances 2013 (No. 3 of 2013) is an Act of the Parliament of Zambia enacted in 2013. It contains 79 sections. Read its sections below, or ask Levy any question about the Medicines and Allied Substances 2013 (No. 3 of 2013) and get an answer grounded in the Act with citations.
Sections of the Medicines and Allied Substances 2013 (No. 3 of 2013)
- S. 1Short title
- S. 2Interpretation
- S. 3Continuation and re-naming of Pharmaceutical Regulatory
- S. 4Seal of Authority
- S. 5Functions of Authority
- S. 6Powers of Authority
- S. 7Constitution of Board of Authority
- S. 8Functions of Board
- S. 9Expert Advisory Committee
- S. 10Committees
- S. 11Delegation of functions of Board
- S. 12Director-General
- S. 13Immunity
- S. 14Prohibition of operation of unregistered pharmacy, health
- S. 15Application for certificate of registration
- S. 16Issue of certificate of registration
- S. 17Rejection of application
- S. 18Display of certificate of registration
- S. 19Annual return
- S. 20Surrender of certificate of registration
- S. 21Transfer of certificate of registration
- S. 22Amendment of certificate of registration
- S. 23Suspension or cancellation of certificate of registration
- S. 24Closure of pharmacy
- S. 25Loss of certificate of registration
- S. 26Management of hospital pharmacies
- S. 27Standard of pharmacy practice
- S. 28Dispensing certificate
- S. 29Agro-veterinary shop permit
- S. 30Health shop permit
- S. 31Register of Pharmacies, Agro-veterinary Shops and
- S. 32Publication of registered pharmacies, agro-veterinary
- S. 33Prohibition of manufacture, distribution, etc. medicine or
- S. 34Pharmaceutical licence
- S. 35Import permit
- S. 36Export permit
- S. 37Additional requirements for import or export for narcotic
- S. 38Register of Licences and Permits
- S. 39Marketing authorisation
- S. 40Categories of medicine
- S. 41Medicines list
- S. 42Prohibition of sale of prescription only medicines without
- S. 43Labelling of medicine
- S. 44Sale of medicine, etc.
- S. 45Advertising of medicines
- S. 46Recall of medicine, etc. from circulation
- S. 47Monitoring medicine and allied substance
- S. 48Register of Marketing Authorisations
- S. 49Prohibition of conducting clinical trial without certificate
- S. 50Application for clinical trial certificate
- S. 51Grant of certificate
- S. 52Inspection of clinical trial sites
- S. 53Register of Clinical Trial Certificate
- S. 54National Drug Quality Control Laboratory
- S. 55Inspectors
- S. 56Appeals
- S. 57Authority to manufacture patented medicine
- S. 58General offences
- S. 59Prohibition of manufacture, import, export, etc of sub-
- S. 60Prohibition of supply of expired medicine
- S. 61Prohibition of deceptive act
- S. 62Prohibition of sale, etc of harmful cosmetics
- S. 63Sale and preparation of cosmetics under insanitary
- S. 64Standards of cosmetics
- S. 65Prohibition of sale of harmful devices
- S. 66General penalty
- S. 67Offence by body corporate or unincorporate body
- S. 68Guidelines
- S. 69Regulations
- S. 70Repeal of Act No. 14 of 2004
- S. IPRELIMINARY
- S. IITHE ZAMBIA MEDICINES REGULATORY AUTHORITY
- S. IIIREGISTRATION AND REGULATION OF PHARMACIES, HEALTH SHOPS AND AGRO-VETERINARY SHOPS
- S. IVLICENCIES, IMPORT AND EXPORT PERMIT
- S. IXGENERAL PROVISIONS
- S. VREGISTRATION OF MEDICINES AND ALLIED SUBSTANCES
- S. VIREGULATION OF CLINICAL TRIALS
- S. VIITHE NATIONAL DRUG QUALITY CONTROL LABORATORY
- S. VIIIINSPECTIONS