by TrN2016_SandWich | Apr 12, 2016
Charles Phillips Charles has extensive experience in medical leadership of face to face meetings with regulators in the US, UK, Canada and Australia. Providing the clinical overview for registration filings of a biologic product, Type II variations on existing...
by TrN2016_SandWich | Apr 12, 2016
Janet Worrell Janet is a pharmacist with a PhD in medicinal chemistry, alumni Manchester and Strathclyde respectively. She has worked in Regulatory Affairs supporting drug development from scientific advice through early phase development (clinical & technical) to...
by TrN2016_SandWich | Apr 12, 2016
Jaminder Khinder A highly experienced Drug Development Scientist with 25 years experience in nonclinical drug safety and nonclinical regulatory for small molecules and biotherapeutics at GlaxosmithKline and Pfizer. Expertise in nonclinical project lead roles with...
by TrN2016_SandWich | Apr 12, 2016
Alan Harris Alan Harris graduated from Southampton University and began his career as a graduate medicinal chemist with Allen and Hanburys (now part of GSK) at their site in Ware, Hertfordshire. During this time he completed a part time MPhil degree on the synthesis...
by TrN2016_SandWich | Apr 12, 2016
Stuart Levy Stuart G. Levy, PhD, has provided chemistry consulting services to the pharmaceutical industry as an independent consultant since 2010. Dr. Levy has more than 18 years of experience in the pharmaceutical industry, primarily at start-up and medium size...
