Kimberly Remillard
Kimberly Remillard has over 20 years of experience in GxP-regulated industries, with a focus on laboratory software, software as a medical device (SaMD), and biotechnology. She has held a range of quality and regulatory roles spanning clinical feasibility, product development, and manufacturing. Kimberly is regulatory affairs certified (RAC) and currently serves as a senior regulatory affairs manager at Thermo Fisher Scientific.
Articles by Kimberly Remillard
Digital transformation is accelerating in regulated labs, forcing leaders to rethink how they manage compliance, data integrity, and oversight
| 4 min read
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