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All ZFDA Documents

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GUIDELINES FOR SUBMISSION OF DOCUMENTATION FOR REGISTRATION OF IN VITRO DIAGNOSTIC DEVICES

File Size 607.20 KB
Downloads 108
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guidelines for registration of premises and licensing of pharmaceutical business

File Size 306.73 KB
Downloads 289
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GUIDELINES FOR PHARMACEUTICAL INSPECTION

File Size 981.79 KB
Downloads 119
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GUIDELINES FOR MEDICAL VIGILLANCE

File Size 605.90 KB
Downloads 30
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GUIDELINES FOR IMPORTATION AND EXPORTATION OF MEDICAL DEVICES INCLUDING IN VITRO DIAGNOSTICS

File Size 355.82 KB
Downloads 38
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GUIDELINES FOR APPLICATION TO CONDUCT CLINICAL TRIALS IN ZANZIBAR

File Size 1.09 MB
Downloads 45
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GUIDELINE FOR REPORTING SAFETY DATA IN CLINICAL TRIALS

File Size 408.53 KB
Downloads 18
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GUIDELINE FOR INDEMNITY AND INSURENCE OF CLINICAL TRIAL IN ZANZIBAR

File Size 413.97 KB
Downloads 33
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GUIDELINE FOR CONDUCTING GOOD CLINICAL PRACTICE (GCP) AND GOOD CLINICAL LABORATORY PRACTICES (GCLP) INSPECTION

File Size 498.67 KB
Downloads 16
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Guideline for Application Business Permit of Medical Devices

File Size 284.10 KB
Downloads 52
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