Page d'accueil  |  Aide  |  Effacer
Anglais  |  Français
 Rechercher  |  Catégories  |  Titres A-Z  |  Pays  |  Comparer pays  |  Index  
Etendre sommaire
Document complet
Dérouler chapitre
Préférences

fermer ce livreA 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)
Afficher le documentForeword
fermer ce répertoireA. The Tanzania National Drug Policy
Afficher le document1. Background
Afficher le document2. Initial Activities
fermer ce répertoire3. Tanzania National Drug Policy 1991
Afficher le documentI. Introduction*
fermer ce répertoireII. Drug Availability
Afficher le document1. Drug selection
Afficher le document2. Drug procurement
Afficher le document3. Distribution
Afficher le document4. Quality assurance
ouvrir ce répertoire et afficher son contenuIII. Rational Drug Use
ouvrir ce répertoire et afficher son contenuIV. National Pharmaceutical Production
ouvrir ce répertoire et afficher son contenuV. Traditional Medicine
Afficher le documentVI. Intersectoral Cooperation
Afficher le documentVII. Technical Cooperation with Other Countries
Afficher le documentVIII. Financial Resources
Afficher le documentIX. Legislation
Afficher le document4. Notes of clarification on some statements in the National Drug Policy document
ouvrir ce répertoire et afficher son contenuB. The Masterplan for the Pharmaceutical Sector of Tanzania Mainland 1992 - 2000
ouvrir ce répertoire et afficher son contenuC. Hospital Therapeutic Committees
 
4. Quality assurance

a. The aim of the National Drug Policy is to ensure that drugs, reaching the patient are safe, effective and of high quality. The quality assurance system will include managerial, technical and legal elements (see notes 5,6 and 7).

b. The drug inspection system will assure that the policy is achieved in all aspects and at all levels of the drug supply system.
The relevant aspects of testing samples will be carried out in national drug control laboratories under the authority of the Government Chemist (see also note 6).

c. All specifications on pharmaceutical products will be stated in laws and regulations (see note 7).

vers la section précédentevers la section suivante

S'il vous plaît envoyez vos commentaires Anglais  |  Français