All Content
CFR 21 part 11 and the electronic registry in the Life Sciences industry
The CFR 21 Part 11 is a standard of the United States Food and Drug Administration (FDA). It establishes the requirements and rules for the use of computerized automation systems in the pharmaceutical, biotechnology, and medical device industries. Therefore, it is widely followed all over the world. The CFR 21 Part 11 guidelines are part … Continue reading “CFR 21 part 11 and the electronic registry in the Life Sciences industry”
Read more