I am working on LIMS (laboratory information management system) domain and I want to learn about the FDA and 21 CFR rules. Can somebody help me in this regard ?
Quote "The 21CFRPart11.com Web site provides access to information on the rule and also maintains an email list that actively discusses issues and concerns with industry peers and government regulators. On this site you will find the latest conference, meeting and seminar information as well as links to vendors and consultants who can help the pharmaceutical community with issues of compliance with regulations and productivity. "