Rich Granquist

Rich Granquist

Speaker

Quality Systems Consultant,

NAMSA

Mr. Granquist has worked in the medical device industry for over 14 years in global quality assurance and EU regulatory affairs. For the last six years, Mr. Granquist has worked for NAMSA Clinical and Consulting as a Quality Systems Consultant. Prior to working at NAMSA, Mr. Granquist worked for Cook Medical as a Quality Engineer and Microbiologist.

He holds an ASQ certification in Biomedical Auditing, and his areas of expertise include Risk Management, Complaint and CAPA investigation, Sterilization Validation, Preclinical Testing and Technical File Management. Recently, he has focused on awareness of the impact of the EU MDR on Quality Systems, Product Development and Risk Management.

Mr. Granquist is a member of the AAMI Quality Management Working Group 04 for the Application of Risk Management to Medical Devices.

My Session

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June 11,2020

Foreseeable Misuse of the New ISO 14971:2019 and EU MDR

11:15 am-12:00 pm

Room 49