21 CFR Part 11 was established in August of 1997, which outlines the FDA’s requirements for electronic records and electronic signatures. These requirements are used to maintain the trustworthiness, reliability and integrity of electronic records. The rule contains two major sections: Electronic Records and Electronic Signatures
Inicio de sesión
¿Aún no está registrado?
Sign up for free today. By registering you will have free access to exclusive content including
- Webinars, presentations and videos
- Application notes, technical notes, articles, white papers and software downloads
And in addition you will receive
- Our regular eNews including the latest news, education, events and offers from Malvern Panalytical