The ever-changing regulatory environment faced by manufacturers in a pharmaceutical setting as well as other regulated industries can cause confusion and doubts about compliance. However, by adopting simplified workflows and incorporating instrument systems specifically designed to meet regulatory requirements it is possible to relieve this burden.
But – how is this achieved?
Watch this webinar to learn how to:- Enable and manage 21 CFR Part 11 in the lab
- Adopt simplified workflows to ensure compliance from each analyst
- 利用内置的性能测试,以确保本月ruments are fit for purpose
