21 CFR Part 11

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Design a compliant lab process control today.

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In order to comply with the FDA’s rules on the manufacturing of human and animal drugs and biologics, 21 CFR Part 11 provides guidance to manufacturers on how to comply with regulation. Our 21 CFR Part 11 white paper details how you can use enteliWEB to comply with 21 CFR Part 11. Use password: cfr1. 

Download 21 CFR Part 11 White Paper

 

Through years of experience in San Diego our automation technology and building technology ensures the optimal temperature for your technology, assets, and most importantly, your talent. 

 

 


Compliance with 21 CFR Part 11 is required for all drug manufacturers in San Diego.