Hi Karen,
Welcome to the group. I think you will find a lot of the information and connections RAPS has to offer very useful. If you have any specific questions, please feel free to reach out to me.
I currently work for Indeio, a medical device consulting company. I am working on a project for a medical device company for EU MDR certification for Class III devices. I have an MS in Regulatory Affairs from Northeastern University and have been full time regulatory for about 6 years, but I have over 15 years experience in the medical device industry. I also have my RAC-Devices certification.
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Liz Bereza, MSRA, RAC-Devices, CMDA
Senior Regulatory Affairs Specialist
Raleigh NC United States
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Original Message:
Sent: 19-Apr-2023 09:11
From: Karen Underwood
Subject: Tell Us About Yourself
Hi Everyone:
A newbie to the group. I work as a Quality Control Compliance Specialist at the University of Maryland Baltimore. I have a BS in Microbiology with Molecular Biology Concentration and a Chemistry Minor. I also have a masters in Regulatory Science. Looking forward to learning and growing with the group.
Karen F. Underwood
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Karen Underwood
Quality Improvement Compliance Specialist
Glen Arm MD
United States
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