Document Revision Log

Document Control cGMP SOP Templates and Supporting Documents

Document Revision Log

AHPA Members log in to access this document

Published: Thursday, April 1, 2010

A form such as this can be used to track the revision of important documents. Such logs can be used for SOPs, labels, formulas, master manufacturing records, etc.  Alternately, this information can be tracked in a spreadsheet or database, or simply on the documents themselves. Tracking this information is not explicitly required by 21 CFR part 111, but may be helpful as a practical matter.
Print

2017 Annual Fund Sponsors

           

AHPA appreciates the support of its sponsors, but does not endorse, recommend, or provide a warranty for any sponsor company, its products or services. AHPA has no responsibility for any transaction entered into with any of these companies.