Dr. William Crumb is a world-renowned expert in ion channel research with CRO experience since 1996, having founded Zenas Technologies, later to become NOVA Research Laboratories. Dr. Crumb provided the hERG data for the ISLI/HESI study which became the foundation for the S7B guidelines. In addition, starting in 2014, Dr. crumb was contracted by the FDA to provide manual ion channel screening in support of the CiPA initiative, the update to the S7B guidelines.
Dr. Crumb received his undergraduate degree from the University of New Orleans and his Ph.D. in Pharmacology from Tulane University School of Medicine, New Orleans. He moved on to a postdoctoral research fellowship in the Department of Molecular Physiology and Biophysics at Baylor College of Medicine, Houston, TX.
Dr. Crumb is author in over 50 peer reviewed journal publications.
Benjamin Butterfield has 19 years business development experience in the pharmaceutical industry. Benjamin served as business director for Chantest Inc. as well as the Toxikon Corporation. Benjamin served as Executive Director of Business Development, North American, for Cyprotex. Under this role Benjamin was involved in merger and acquisition activities including the acquisitions of Cellumen, Apredica and CeeTox Labs by Cyprotex, creating two new brick and mortar US based facilities. These efforts led to the sale of Cyprotex to Evotek in 2016.
Benjamin is trained in preclinical FDA compliance regulations GLP/GMP/ISO. Disease states studied: Pain Management, Neuropathic Pain, and Rheumatoid Arthritis, Neurological disorders, Migraines, Epilepsy, Diabetic Neuropathy, preclinical cardiovascular safety.
Samantha Coffee has over 20 years of analytical experience in both the GLP and GMP regulated laboratory space. She received her Bachelor of Science degree in Biochemistry and Molecular Biology from The Pennsylvania State University, along with a minor in both Chemistry and Microbiology. She has served in laboratory management roles at WIL Research Laboratories, Charles River Laboratories, Cytocentrics, and Ingredients Innovation International. She has extensive knowledge of HPLC instrumentation, as well a great understanding of conducting studies in accordance with Good Laboratory Practice.
Dr. Fossa is an independent scientific consultant in preclinical and clinical cardiovascular safety. Fossa Consulting LLC offers an integrated approach when assessing cardiac safety issues.
Dr. Fossa received his Ph.D. in Pharmacology and Toxicology from Purdue University in 1983 and was employed by Pfizer as a Research Fellow from 1986-2008. During his tenure he helped form the General Pharmacology group in Pfizer Discovery in 1988 and conducted in vivo preclinical cardiovascular assessments on over 150 clinical drug candidates and was a key contributor on 5 NDAs.
Dr. Fossa was one of four original founding members of the General Pharmacology/Safety Pharmacology Steering committee that is known today as the Safety Pharmacology Society. He has authored a diverse range of publications related to cardiovascular assessment and has numerous patents related to novel therapeutic modalities. His research focused on the use of the beat-to-beat dynamics and the ECG QT – TQ interval relationship in humans and conscious dogs, to assess arrhythmia liability related to human QT prolongation. He established several in vivo models to differentiate proarrhythmic liability of drug candidates with emphasis on the impact of changes in autonomic tone. In 2007, he moved to Clinical Translational Medicine at Pfizer to set up beat-to-beat analysis for human use. This work was later commercialized by a joint venture with U. Rochester to form iCardiac Technologies where he was Vice President of Cardiovascular Safety until 2014. During that period, beat-to-beat and ECG restitution analyses were used successfully in several regulatory facing clinical studies for drug approvals. In 2014, Dr. Fossa began working independently as a cardiovascular safety consultant through his own company, Fossa Consulting LLC.
Dr Shah qualified in medicine in 1970 from the St Mary's Hospital Medical School, University of London, and subsequently specialised in internal medicine and cardiology. He is a Fellow of the Royal College of Physicians and a Fellow of the Faculty of Pharmaceutical Medicine. He is also on the Examining Board of the Faculty. Dr. Shah has over 100 publications within his area of expertise.
He was a member of the team that first characterised CYP2D6 and has authored a number of papers on pharmacogenetics. He also the nominated Expert representing the EU/EMEA at the ICH E14 Topic on QT interval and has advised many pharmaceutical companies on QT-liability of drugs and has authored a number of papers on this subject. He is an honorary fellow of the British Pharmacological Society, a fellow of the Royal Society of Medicine and founding member of the Society of Pharmaceutical Medicine.
At the CPMP level, he was active at the Efficacy Working Party and involved in drafting the CPMP guidelines on drug-drug interactions and clinical trials with cardiovascular medicines, particularly chronic heart failure.
Dr. Olivier has been developing drugs for over 15 years and is currently Executive Director of Development at Morphic therapeutics in Waltham, MA. Dr. Olivier’s work experience includes biotechnology and pharmaceutical companies, spending time at Regeneron, Biogen, GlaxoSmithKline, Merrimack, Acceleron and Torque developing diagnostics, small molecule drugs, cell based therapies and biologics for indications in cardiology, neurology, neuromuscular, immunology, rare disease, infectious disease, fibrosis and oncology.
Though his primary duties have been safety evaluations, Dr. Olivier has held the role of Project Leader, Head of Project Management, Head of Regulatory, Head of Pharmacokinetics, Head of Bioanalytical Development, Validation and Sample Analysis and Head of Nonclinical supporting multiple INDs, IMPDs, CTAs, NDAs, BLAs and PLEs. In addition, Dr. Olivier is an adjunct faculty member at Oklahoma State University and has taught drug development courses at OSU, Harvard, MIT and through the American College of Toxicology (former elected Council Member and currently serving on the Editorial Board of the International Journal of Toxicology).
Most recently, Dr. Olivier was elected to serve on Council for the Biotechnology Specialty Section of the Society of Toxicology. Three years ago, he created what is currently the Oklahoma State graduate course on drug development attended largely by faculty, medical and veterinary students. Dr. Olivier’s publications include evaluations of toxicity related to novel therapeutics in immunology and oncology, such as interferons, bispecific antibodies and targeted liposomal nanotherapies. In 2016, he published a book on the development of ADCs covering chapters from discovery through post-market approvals with topics spanning all aspects of drug development, including CMC, Nonclinical, Regulatory and Clinical strategies.
Dr. Mason is Professor of Medicine (Cardiology) at the University of Utah, Chief Medical Officer at Spaulding Clinical Research, and an independent consultant in cardiac safety. He was a member of the Stanford University Faculty in Cardiology from 1975 to 1983. He became Chief of Cardiology at the University of Utah in 1983. In 1999 he was appointed Chairman of the Department of Medicine at the University of Kentucky. From 2003 to 2007 he served as Medical Director and Director of R&D at Covance Cardiac Safety Services. His clinical, teaching and research emphasis is in cardiac arrhythmias, electrocardiography and electrophysiology.