21 CFR Part 11 Conformance for Medical Devices

Date : 30th September 2020 to 30th September 2020

Place : United States, Littleton

Website :https://bit.ly/3iUSsMe

Contact Person:Michael Smith

Description:

FDA regulated companies want to transition to electronic records for economy and efficiency. FDA, because of its concern for patient safety, wants to prevent electronic records from being compromised with possible resulting harm to the patient.

21 CFR Part 11 Conformance for Medical Devices will be held in Littleton,United States on date 2020-09-30

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Deadline for abstracts/proposals : 29th September 2020

Keynote Speakers : Edwin Waldbusser is a consultant retired from industry after 20 years in management of the development of medical devices (5 patents). He has been consulting in the US and internationally in the areas of design control, risk analysis, and software validation for the past 11 years. Mr. Waldbusser has a BS in Mechanical Engineering and an MBA. He is a Lloyds of London certified ISO 9000 Lead Auditor and a member of the Thomson Reuters Expert Witness network.

Check the event website for more details.