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Doc. No.: INS/FOR/067 Revision No.: 2 Effective Date: 10 Nov. 2017National Drug Authority Plot No. 19, Rupee Towers, Mumbai Avenue, P.O. Box 23096, Kampala, Uganda. Email: ndaug@nda.or.ug; website:

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Who needs application form for gmp?

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Companies or organizations involved in manufacturing, processing, packaging, or storing pharmaceutical products that must comply with Good Manufacturing Practices (GMP) regulations.

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Individuals responsible for ensuring that the manufacturing processes and facilities meet the required GMP standards.

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Regulatory authorities that oversee compliance with GMP regulations in the pharmaceutical industry.

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What is application form for gmp?

The application form for gmp is a document used to apply for Good Manufacturing Practice certification.

Who is required to file application form for gmp?

Any company involved in the manufacturing of pharmaceutical products is required to file the application form for gmp.

How to fill out application form for gmp?

To fill out the application form for gmp, companies need to provide detailed information about their manufacturing processes, quality control measures, and compliance with regulations.

What is the purpose of application form for gmp?

The purpose of the application form for gmp is to demonstrate compliance with Good Manufacturing Practices and ensure the quality and safety of pharmaceutical products.

What information must be reported on application form for gmp?

The application form for gmp must include information about manufacturing processes, equipment, facilities, personnel, quality control procedures, and compliance with regulatory requirements.

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