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Revalidation Process in Drug Manufacturing by William DC Rivera is a document available to read on EtoBox.

What is Revalidation Process in Drug Manufacturing about?

Revalidation of process controls, equipment, batch size, API source, and excipient source is conducted: a) annually or after changes are made to the manufacturing process b) after equipment is relocated or significant changes are made c) when scaling up to a larger batch size d) when changing API source or manufacturer e) when changing excipient source or manufacturer

Author

William DC Rivera

Language

EN