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GMP Subject Downloads
1. Site Master File
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2. Checklist GMP-Inspections
650 questions typically asked during audits
3. Process Validation
official requirements, validation planning and procedure, ...
GMP Compliant Documentation
How to create, organize, review and archive GMP related documents in pharmaceutical industries
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News about GMP/cGMP
Regulatory Roundup: FDA Reorganizes the Office of the Commissioner, more....
FDA also announced in the Aug. 18 Federal Register an extension of the public period for its transparency initiative. FDA’s Transparency Task Force is looking for industry’s feedback on ways it can be more open about agency activities and expectations.
To read more about the article follow the link below:
Link to PharmTech.com