Medicine and Cosmetics Guidelines
GUIDELINES ON VARIATIONS ON REGISTERED MEDICINAL PRODUCTS
GUIDELINES ON SUBMISSION OF DOCUMENTATION FOR RENEWAL OF MARKETING AUTHORIZATION OF HUMAN AND VETERINARY MEDICINAL PRODUCTS
GUIDELINES FOR EMERGENCY USE AUTHORIZATION OF MEDICINAL PRODUCTS
GUIDANCE ON PROCESSING OF APPLICATIONS FOR REGISTRATION OF MEDICINAL PRODUCTS THROUGH NON-ROUTINE PROCEDURE IN ZANZIBAR
MEDICINE EVALUATION AND REGISTRATION COMPENDIUM
GUIDELINES ON SUBMISSION OF APPLICTION FOR REGISTRATION OF MEDICAL DEVICES
GUIDELINES FOR SUBMISSION OF DOCUMENTATION FOR REGISTRATION OF IN VITRO DIAGNOSTIC DEVICES
guidelines for registration of premises and licensing of pharmaceutical business
GUIDELINES FOR PHARMACOVIGILANCE SYSTEM STRENGTHENING
GUIDELINES FOR PHARMACEUTICAL INSPECTION
GUIDELINES FOR MEDICAL VIGILLANCE
GUIDELINES FOR IMPORTATION AND EXPORTATION OF PHARMACEUTICAL
GUIDELINES FOR IMPORTATION AND EXPORTATION OF MEDICAL DEVICES INCLUDING IN VITRO DIAGNOSTICS
GUIDELINES FOR APPLICATION TO CONDUCT CLINICAL TRIALS IN ZANZIBAR
GUIDELINE FOR REPORTING SAFETY DATA IN CLINICAL TRIALS
GUIDELINE FOR PHARMACIST INTERNSHIP TRAINING
GUIDELINE FOR INDEMNITY AND INSURENCE OF CLINICAL TRIAL IN ZANZIBAR
GUIDELINE FOR CONDUCTING GOOD CLINICAL PRACTICE (GCP) AND GOOD CLINICAL LABORATORY PRACTICES (GCLP) INSPECTION
Guideline for Application Business Permit of Medical Devices