How 21 CFR Part 11, the FDA regulation pertaining to use of electronic records and signatures, and the HIPAA electronic security regulations for patient medical records fit into the validation process
The latest computer system industry standards for data transfer, data security, and audit trails
How to streamline SOP revision, authoring, approval and review
Recent FDA inspection trends
Who should Attend
Clinical, regulatory and IT professionals working in the clinical trial, health care, medical device and biopharmaceutical sectors.
Past Events
Computer System Validation - Reduce Costs and Avoid 483s 2017 - 09-10 Oct 2017, Radisson Blu Royal Viking Hotel, Stockholm, Sweden (34507)
Computer System Validation - Reduce Costs and Avoid 483s 2017 - 14-15 Sep 2017, Philadelphia Marriott Downtown, Pennsylvania, United States (34506)
Computer System Validation - Reduce Costs and Avoid 483s 2016 - 08-09 Sep 2016, Philadelphia, Pennsylvania, United States (30101)
Computer System Validation - Reduce Costs and Avoid 483s 2016 - 04-05 Feb 2016, DoubleTree by Hilton Hotel San Diego Downtown, California, United States (55538)
Computer System Validation - Reduce Costs and Avoid 483s 2026
Important
Please, check "Computer System Validation - Reduce Costs and Avoid 483s" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Medical device, Medical laboratories, Pharma
