MEDIcept Inc.
- Gregg V.
Gregg V. is a seasoned professional with extensive experience in software quality engineering, risk management, and clinical research within the medical device industry. Currently serving as a Sr. Software Quality Engineer at MEDIcept Inc. since April 2023, Gregg previously held roles at Advanced Bionics as Principal Systems Engineer, where an enterprise-wide risk management system was developed, and Beckman Coulter as Product Safety Risk Manager, focusing on compliance with international standards. Earlier positions include Manager of Product Safety Risk Management at Medtronic Diabetes, where strategies for risk management processes were established, and Sr. Clinical Research Specialist at Medtronic Diabetes, responsible for clinical research training. Additional experience encompasses roles in research at City of Hope and Keck School of Medicine, with a doctoral background in Physiology and Biophysics from the University of Southern California, complemented by degrees in Human Nutrition and Mathematics.
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MEDIcept Inc.
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MEDIcept strives to provide our clients with proven, trusted, and cost-effective solutions. We are an international medical device, IVD, combination product, and biotechnology compliance consulting firm. For over 25 years, our unique consulting practice has assisted thousands of companies of all sizes with cost-effective Regulatory, Quality, Clinical, Auditing, and Educational services. Our experienced team of former FDA, Notified Body, and industry experts will work with you to efficiently develop or remediate a quality system, create a regulatory strategy, or establish a clinical trial, to meet your specific needs. MEDIcept will help you navigate the complex FDA and international regulatory pathways, reduce business risk, and decrease time-to-market while maximizing your potential for success. Every client and every issue is unique. We customize our solutions to fit your needs. With a retention rate of over 90%, we can promise that you will benefit from working with us.
