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Document No. QA001×2010 Date of I SSR e : 01 01 201 1 Rev I is o n D a t e : 0 1 0 1 2 0 1 2 Quality Policy Directorate General of Drug Administration is committed to protect the health of people
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Dgda pdf stands for Drug Control Authority pdf, which is a form used to report information related to drugs and pharmaceutical products.
Manufacturers, importers, distributors, and retailers of drugs and pharmaceutical products are required to file dgda pdf.
Dgda pdf can be filled out online or manually by providing accurate information about the drugs and pharmaceutical products being reported.
The purpose of dgda pdf is to ensure compliance with regulations, monitor the distribution of drugs, and maintain the safety of pharmaceutical products.
Information such as drug name, batch number, quantity, manufacturing date, expiration date, and distributor details must be reported on dgda pdf.
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