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Complying with US FDA Title 21 CFR Part 11 for the Life Sciences Industry


Source: SAP


Document Type: White Paper

Description:

Compliance with US FDA regulations is a market requirement. Thus, among the nearly 1,500 installations of mySAP ERP software among pharmaceutical, medical diagnostics and devices, and biotechnology companies worldwide, it is vital to be aware of the functions and features of mySAP ERP that demonstrate technical compliance with US FDA 21 CFR Part 11 Electronic Records; Electronic Signatures; Final Rule.


Download <strong>Complying with US FDA Title 21 CFR Part 11 for the Life Sciences Industry</strong>
 

Comments:
Related Topics:  Process Manufacturing, Regulatory and Compliance

 Related Industries:  Food and Beverage Products, Pharmaceutical and Botanical Products

 Related Keywords:  SAP, mySAP ERP, FDA compliance, US FDA 21 CFR Part 11, Electronic Records, Electronic Signatures, Final Rule, life sciences industry, good manufacturing practices, GMPs

 Source: SAP
Learn more about SAP


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