Validant
Lawrence Mainwaring is an accomplished EU MDR Specialty Content Author at Validant, where responsibilities include rewriting CE Technical files to align with new MDR regulations while collaborating with subject matter experts to ensure compliance. Previous experience includes roles as an Advanced Manufacturing Engineer at Medtronic, where manufacturing equipment installation and qualification for scale-up activities were key duties, and as a Senior Preclinical Scientist at Sapheon, managing biocompatibility studies and authoring toxicological risk assessments. Additional expertise was developed at Ethicon in various positions, including Preclinical Scientist and Senior Associate Scientist, contributing to the successful launch of significant medical products. Earlier in the career, Lawrence worked as a Chemist III at Closure Medical, leading stability studies and developing formulations. Academic credentials include a Master of Science in Biology from East Tennessee State University and a Bachelor of Arts in Biology from the University of North Carolina Asheville.
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Validant
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Validant is a full-service life science consulting firm serving developers and manufacturers of pharmaceuticals, biologics, medical devices, and diagnostics worldwide. We partner with these companies to ensure safe and reliable access to life-saving healthcare products, facilitating their efficient, compliant progression from preclinical and clinical phases through to manufacturing and distribution—and optimizing quality at each step. Our platform brings together leading specialists in each facet of the product lifecycle, and we have curated an extensive and diverse global network of consultants to help execute strategies worldwide. Because of this, Validant is able to deliver our breadth of consulting, execution, and support services in the right place, at the right level, and in the right combination to meet your exact need. We've empowered hundreds of clients – from start-ups to the largest global leaders – to efficiently navigate regulatory, compliance, and quality complexities. How can we help you?