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FDANews Webinar:

Sustained Medical Device Regulation Compliance: Ensure Your Regulatory Processes and Tools are Fully Optimized

Featured Speakers

Kim Young

Kim Young, Instem’s Director, Global Regulatory Intelligence, is a 20-year regulatory affairs professional. As Instem’s subject matter expert, she is responsible for monitoring market dynamics and ensuring key requirements are an integral part of Instem’s product strategy and development activities. Ms. Young has held key regulatory operations roles across the medical device, pharmaceutical and personal care product industries. She received a Graduate Certificate in Medical Devices and MSc in Regulatory Affairs, Drugs, Biologics and Medical Devices from Northeastern University.

Chris Nichols

Chris Nichols, a 15-year veteran of life sciences and regulatory affairs spanning preclinical through late stage clinical, is a  Application Specialist at Instem. In this role, he works closely with organizations to understand their unique regulatory requirements and helps implement Instem’s beneficial solutions. Mr. Nichols received a BS in computer science from Iowa State University and a Masters in Business Administration from the University of St Thomas.