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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)
Open this folder and view contents4. Pharmacy Board
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
 

5. Drug Quality Assurance and Control

It is essential that drugs, reaching the patient are safe, effective and of high quality. It has been mentioned before that drug registration and drug inspection are important tools to ensure this. It however also needs the support of laboratories, capable to perform quality control on drugs. In many countries unscrupulous persons try to penetrate the drug market with counterfeit or fake Pharmaceuticals. This is a serious criminal offence as it endangers life of innocent people. Authorities and health professionals have to be on the alert permanently. It is therefore essential to establish drug quality control facilities, linked with the Pharmacy Board and the Government Chemist.

As mentioned before standards for pharmacy practise and GMP are elements contributing to quality assurance, but they are also in need of additional support from laboratory facilities. The development of adequate reliable drug quality control laboratory services is therefore included in the Masterplan.

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