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CAMP Regulationshttp://www.fda.gov/cder/dmpq/cgmpregs.htm21 Code of Federal Regulations Parts 210 and 211 Part 210 CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING

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What is part 211 - current?

Part 211 - current refers to the regulations set forth by the Food and Drug Administration (FDA) regarding good manufacturing practices for finished pharmaceuticals.

Who is required to file part 211 - current?

Manufacturers of finished pharmaceutical products are required to comply with and file part 211 - current.

How to fill out part 211 - current?

Part 211 - current must be filled out by following the guidelines provided by the FDA in the regulations.

What is the purpose of part 211 - current?

The purpose of part 211 - current is to ensure the quality and purity of pharmaceutical products that are manufactured and sold in the United States.

What information must be reported on part 211 - current?

Part 211 - current requires manufacturers to report information related to the production, testing, and quality control of pharmaceutical products.

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