Peter Murray has recently retired as a Quality Director at GSK after 45 years’ experience of Primary and Secondary Pharmaceutical Manufacture with experience concentrated in the areas of Quality Assurance and GMP compliance. The past 20 years have involved significant international experience, at Quality Director Level, of delivering effective Quality and Compliance management of GSK sites and 3rd Party contract manufacturers and developing long term strategies for the quality management of manufacturing sites. He is registered as an eligible Qualified Person and is a member of the MC2 British Pharmacopoeia expert advisory committee.

A keen analyst with an experience of about 13 years and above, experience in Analytical Research and Quality management, Testing & Inspection, Lab Operation as well as Compliance in the Pharmaceutical Sector. Expertise in designing and implementing procedures for ensuring adherence to the quality standards. Possess a clear understanding of the pharmaceutical industry, technology trends and quality control techniques. Well acquainted with quantitative and qualitative analysis of compounds by chemical and instrumental too. Conversant with pharmacopoeia (USP, Ph.Eur, BP). Have handled APIs, Excipients and oral dosage forms.

Dr. Christopher Joseph Devine is the President of Devine Guidance International, Inc., a consulting firm specializing in providing solutions for regulatory compliance, quality control, supplier audits, internal audits, and supplier management issues facing the medical device industry. Additionally, Dr. Devine is the author of Devine Guidance, a weekly blog focusing on the understanding of regulations mandated by the FDA and other regulatory bodies; and published by the Medical Device Summit. Furthermore, Dr. Devine is the author of three books on regulatory compliance. Dr. Devine has 34-years of experience in quality assurance, regulatory affairs, and program management. He is a senior member of the American Society for Quality (ASQ), a member of Regulatory Affairs Professionals Society (RAPS), a member of the Project Management Institute (PMI), and a member of the Society of Manufacturing Engineers (SME).

J. Lawrence Stevens, RAC has a unique background of FDA and private industry experience. He has over 20 years of FDA experience encompassing virtually all of the FDA field positions. He also has eighteen years of industry experience as a mid-level manager and senior executive in clinical, regulatory, and quality in the medical device industry. Her personally designed quality systems, prepared regulatory submissions (510(k), IDE and PMA) and managed 7 multi-center clinical trials for class 3 medical devices. He has published articles in peer journals on managing clinical trials, and design control for medical devices.