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FDA/SMC/SD/GLS MP/2015/05FOOD AND DRUGS AUTHORITYGUIDELINES FOR SAFETY MONITORING OF MEDICINAL PRODUCTSDocument No. Date of First Adoption: FDA/SMC/SD/GLS MP/2015/05 : 19thDecember 2015Version No.:
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Who needs food and drugs authority?

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The food and drugs authority is needed by various entities and individuals involved in the production, distribution, and sale of food and drugs. The following may require services from the food and drugs authority:
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- Food manufacturers and processors
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- Pharmaceutical companies
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- Drug manufacturers and distributors
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- Importers and exporters of food and drugs
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- Retailers and wholesalers of food and drugs
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- Healthcare facilities like hospitals and clinics
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- Research institutions
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These entities and individuals rely on the food and drugs authority to ensure the safety, quality, and legality of food and drugs in their respective jurisdictions.
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Food and Drugs Authority (FDA) is a regulatory agency responsible for overseeing the safety and efficacy of food and drugs in a country.
Manufacturers, distributors, importers, and exporters of food and drugs are required to file with the FDA.
To fill out the FDA, companies need to provide information on the products being sold, ingredients used, manufacturing processes, and any relevant testing and certifications.
The purpose of the FDA is to ensure that food and drug products in the market are safe, effective, and of high quality for consumers.
Information such as product details, ingredients, manufacturing processes, testing results, certifications, and contact information must be reported on the FDA.
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