UK
English (GB)

21 CFR Part 11

Since its inception in 1997, the Food and Drug Administration’s (FDA) standards for Title 21 of the Code of Federal Regulations (CFR) — otherwise known as FDA 21 CFR— have undergone revisions to deliver a set of clear and concise regulations.
Contact us
Our experts are here to help configure the optimal monitoring solution for your environment.
Modification de documents