James has in excess of 25+ years regulatory experience in the OTC sector of the industry. His background covers a wide spectrum of areas including regulatory strategy and implementation, reclassifications, borderline products, promotional copy approval, medical devices and pharmacovigilance. He has worked with major pharmaceutical companies and a wide scope of entrepreneurial clients. To achieve success one has to work with the legislation and apply innovative strategy. This thinking outside of the box approach is a one which has been well received and appreciated. The goal is always delivery of the right end point and not just task delivery. James has a degree in Applied Biology and is a Fellow of TOPRA.
Dr Harriet Scorer
Harriet has worked in medical affairs in the OTC industry for more than 25 years as a medical director at a global OTC company, and latterly consulting to clients including large international ones, SMEs and start-ups. She has been a member of the Medicines Commission and Health Select Committee advisor and has experience of switches, NPD, product launches, medical devices, pharmacovigilance, claims development and copy approval.
Janet began crafting her regulatory skills at Thomas Kerfoot and Medeva in Ashton under Lyne, before moving to 3M as the global regulatory lead for Qvar. Her first role in OTC medicines began at Boots the Chemists, gaining approval of new consumer medicines for the new Republic of Ireland stores, before transferring to senior roles within Boots Healthcare International, supporting Strepsils globally. Operational roles combined with Global Regulatory responsibilities saw a return to inhaled drug development with Vectura. Latterly at Boots Pharmaceuticals she was the Head of Innovative Regulatory Affairs, assessing solutions for consumers in healthcare, covering food supplements through to reclassification strategies. She runs regular food supplement networking events with Medilink East Midlands.
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