Computer System Validation Seminar Announced by ComplianceOnline

Sept. 8, 2011 - PRLog -- ComplianceOnline, a leading provider of FDA regulatory/ compliance trainings will conduct a RAPS certified 2-day seminar from October 20-21, 2011 in Philadelphia, PA, on Computer System Validation: Reduce Costs and Avoid 483s.

The seminar will train companies in FDA regulated industries on proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments. Attendees can learn how to decrease software implementation times and lower costs using a 10-step risk-based approach to computer system validation.

For more information or to register for the seminar, please click here.

This interactive 2-day in-person workshop will address the latest computer system industry standards for data security, data transfer, and audit trails. Attendees will learn how 21 CFR Part 11, the FDA regulatory compliance  pertaining to use of electronic records and signatures, and the HIPAA electronic security regulations for patient medical records fit into the validation process.

Finally, the instructor, David Nettleton, will review recent FDA inspection trends and discuss on how to streamline SOP authoring, revision, review, and approval.

The seminar will benefit anyone that uses computer systems to perform their job functions and is ideal for regulatory, clinical, and IT professionals working in the health care, clinical trial, biopharmaceutical, and medical device sectors.

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