At SMPV Limited, our strength lies in deep, hands-on experience across drug safety, clinical development, and regulatory compliance. Led by Stephanie Martin, we bring strategic insight and operational clarity to every engagement, helping biopharma teams build inspection-resilient systems that scale with confidence.

With over 25 years in the pharmaceutical industry, Stephanie has supported global organisations in designing, optimising, and sustaining PV and QA systems that meet the highest regulatory standards. Her career spans drug safety, clinical operations, and quality management, with a focus on inspection readiness and system transformation.
Stephanie is known for her integrity, pragmatic approach, collaborative style, and ability to translate complex regulatory requirements into practical, scalable solutions. She is committed to high quality results and has successfully supported MHRA, EMA, and FDA inspections to name a few. She continues to be a trusted advisor to PV and QA leaders navigating change, growth, and compliance challenges.
SMPV Limited
London, United Kingdom
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