FDA 21 CFR Part 11 outlines how an organisation can use electronic records and signatures in place of paper-based documents so that it complies with FDA regulations. You can learn more about FDA 21 CFR Part 11 here.
FDA 21 CFR Part 11 outlines how an organisation can use electronic records and signatures in place of paper-based documents so that it complies with FDA regulations. You can learn more about FDA 21 CFR Part 11 here.
Laboratory equipment maintenance, repair, calibration and sales.
