Validating computerized systems is required to demonstrate adherence to data integrity, says Susan J. Schniepp, distinguished fellow at Nelson Laboratories, LLC. Q. I ...

Analytical equipment should be qualified and computer systems should be validated to demonstrate suitability for the intended use. Electronic records must comply with FDA Part 11 and EU/PICS GMP Annex ...

System documentation should include a system description, history, validation information, and references, according to Siegfried Schmitt, Vice President, Technical at Parexel. Q. Some 10 years ago, ...

Dublin, May 14, 2025 (GLOBE NEWSWIRE) -- The "Risk-based Computer System Validation; Reduce Costs and Avoid 483s (ONLINE EVENT: August 6-7, 2025)" has been added to ResearchAndMarkets.com's offering.

Dublin, Aug. 25, 2025 (GLOBE NEWSWIRE) -- The "Digital Validation Demystified - GAMP? 5 2.0 and CSA Integration" training has been added to ResearchAndMarkets.com's offering. This course equips you ...