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THE UNITED REPUBLIC OF TANZANIACHAPTER 219 TANZANIA MEDICINES AND MEDICAL DEVICES ACT [PRINCIPAL LEGISLATION] REVISED EDITION OF 2021This Edition of the Tanzania Medicines and Medical Devices Act,

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Anyone in Tanzania who requires medical treatment or prescription medication would need Tanzania medicines and medical services.

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What is tanzania medicines and medical?

Tanzania Medicines and Medical Agency (TMDA) is responsible for regulating the quality, safety, and efficacy of medicines and medical devices in Tanzania.

Who is required to file tanzania medicines and medical?

All pharmaceutical companies, medical device manufacturers, importers, and distributors in Tanzania are required to file with TMDA.

How to fill out tanzania medicines and medical?

Companies need to submit an application and relevant documentation to TMDA, including details about the products being imported or manufactured.

What is the purpose of tanzania medicines and medical?

The purpose is to ensure that medicines and medical devices in Tanzania meet the required standards for quality, safety, and efficacy.

What information must be reported on tanzania medicines and medical?

Companies must report details about the products being imported or manufactured, including ingredients, dosage forms, and packaging.

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