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REPUBLIC OF BOTSWANA MINISTRY OF HEALTHApplications to be sent to: Director of Health Services/o Drugs Regulatory Unit (DR) Ministry of Health P/Bag 0038 Gaborone Attention: Chief PharmacistAPPLICATION
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What is c/o Drugs Regulatory Unit (DRU) Form?

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c/o Drugs Regulatory Unit (DRU) template instructions

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Co Drugs Regulatory Unit is a department responsible for overseeing and regulating pharmaceutical products.
Pharmaceutical companies and manufacturers are required to file the co drugs regulatory unit.
To fill out the co drugs regulatory unit, companies need to provide detailed information about their pharmaceutical products, manufacturing processes, and any adverse events.
The purpose of co drugs regulatory unit is to ensure the safety, efficacy, and quality of pharmaceutical products in the market.
Companies must report information such as drug ingredients, manufacturing processes, adverse events, and any changes to the product.
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