FDA regulation training for electronic record system using 21 CFR Part 11 Compliance to address patient safety

Date : 4th May 2016 to 4th May 2016

Place : United States, New hyde park

Website :https://complianceglobal.us/product/700286/HowardTCooper/developing-the-quality-system/1

Contact Person:Compliance Global Inc.

Description:

FDA regulation training for electronic record system using 21 CFR Part 11 Compliance to address patient safety

FDA regulation training for electronic record system using 21 CFR Part 11 Compliance to address patient safety will be held in New hyde park,United States on date 2016-05-04

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Deadline for abstracts/proposals : 4th May 2016

Keynote Speakers : Edwin Waldbusser retired from industry after 30 years in management of development of medical device products and development of company Quality Systems. Products included IVD devices, kidney dialysis systems and inhalation devices. His QS experience includes design control, risk analysis, CAPA, software validation, supplier qualification/control and manufacturing/non-conforming product programs. Ed has a B.S. Mechanical Engineering from NYU and a M.B.A from Drexel University. He is certi

Conference Highlights :Overview: This Webinar will explain what 21 CFR Part 11 training is, why it is important to c companies and how conformance to Part 11 differs from just having good IT security. Procedures for controlling electronic signatures and electronic records will be explained. FDA regulation training is required for companies who want to transition to electronic record system for economy and efficiency. FDA, because of its concern for patient safety, wants to prevent electronic records from being c

Venue :Compliance Global Inc., 2754 80th Avenue, New Hyde Park, NY 11040, United States

Check the event website for more details.