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2013 New GMP A Risk based Approach Features : Practical GMP New Risk Assessment Cases Quality System Validation Interactive program Science Corporation June 2324, 2013 Le Passage Cairo Hotel www.progamma.ca
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What is new gmp a?
New GMPA stands for New Good Manufacturing Practice Application.
Who is required to file new gmp a?
Manufacturers or distributors of pharmaceutical products are required to file New GMPA.
How to fill out new gmp a?
New GMPA can be filled out online through the designated government portal by providing all necessary information and documentation.
What is the purpose of new gmp a?
The purpose of New GMPA is to ensure that pharmaceutical products are manufactured and distributed following Good Manufacturing Practices to guarantee quality and safety.
What information must be reported on new gmp a?
Information such as manufacturing processes, quality control measures, facility details, and product specifications must be reported on New GMPA.
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