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close this bookA Short Information Manual on: The Tanzania National Drug Policy, The Master Plan for the Pharmaceutical Sector 1992-2000 Tanzania Mainland - A Summary, Hospital Therapeutic Committees (WHO; 1993; 42 pages)
View the documentForeword
Open this folder and view contentsA. The Tanzania National Drug Policy
close this folderB. The Masterplan for the Pharmaceutical Sector of Tanzania Mainland 1992 - 2000
View the document1. Introduction
View the document2. Central Medical Stores (CMS)
View the document3. Pharmaceuticals and Supplies Unit (PSU)
close this folder4. Pharmacy Board
View the document4.1. General
View the document4.2. Drug Legislation
View the document4.3. Drug Registration
View the document4.4. Drug Inspection
View the document4.5. Drug Information
View the document4.6. Drug Advertising and Promotion
View the document5. Drug Quality Assurance and Control
View the document6. Local Production of Pharmaceutical Products
View the document7. Traditional Medicine
View the document8. Local Financing of Drugs
View the document9. Conclusions
Open this folder and view contentsC. Hospital Therapeutic Committees
 

4.2. Drug Legislation

The present Pharmaceuticals and Poisons Act (1978) is outdated. It is partly a reflection of the pre-second world war legislation in the UK and it is not providing an adequate legal basis to support and enforce implementation of the National Drug Policy. It will therefore be replaced by a new modern Act. This Act will consider fundamental essential requirements as well as constraints in their implementation, caused by the prevailing conditions in the Tanzanian Health Sector.

The Act will give an appropriate framework within which the Pharmacy Board can operate effectively. The Board should thus become a properly functioning drug regulatory authority, which ensures that all pharmaceutical products conform to acceptable standards of quality, safety and efficacy and that all premises and machines for manufacturing, storing and distributing these products comply with requirements, so that drugs reaching the patients are safe and effective.

Three main activities will fall under the direct authority of the Board:

- Drug Registration
- Drug Inspection
- Drug Information.

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