Development of Biopharmaceutical Drug-Device Products

26.08.2021

Englisch

9783030314170

Springer International Publishing

AAPS Advances in the Pharmaceutical Sciences Series

Nein

893

1st edition 2020

Taschenbuch

Feroz Jameel heads the formulation development function of New Biological Entities at AbbVie, Lake County, IL, where he is involved in early and late stage development of parenteral products. Prior to joining AbbVie, Feroz worked at Baxter Biosciences and Amgen. At Baxter, Feroz was involved in the end-to-end development and tech transfer of recombinant Factor VIII (RecombinateTM). At Amgen, Feroz worked over several years in the Parenteral Delivery Drug Product and Process Development where he was involved in the drug product development and tech transfer of several parenteral products including Enbrel®, Nplate®, Repatha® and Blincyto®. Feroz received his Master’s degree in Pharmaceutics from the University of Delhi and Ph.D. in Pharmaceutics (Pharmaceutical Sciences) from the University of Connecticut. His publications include over 20 peer-reviewed manuscripts, over 20 presentations, and several book chapters. He is the co-editor of the books “Formulation and ProcessDevelopment Strategies for Manufacturing of Biopharmaceuticals” and “Quality by Design for Biopharmaceutical Drug Product Development”. He has held several leadership positions at the AAPS including chair of “Freezing and Drying Technologies” and led the industrial consortium for Lyo QbD. Currently, he is leading the industrial consortium on “Best practices/guidelines for validation of Lyophilization process and products”. He is a recipient of 2 patents in lyophilization formulation and lyophilization process development. In addition to corporate awards, Henry Kramer from Baxter and Volwiler Award from AbbVie, Feroz received several awards including the AAPS and PDA’s Fred Simon’s award for the best paper published in the PDA Journal of Pharmaceutical Science and Technology. He has also chaired several symposia on the development of biological products. John Skoug has more than 30 years of pharmaceutical industry experience and specializes in CMC product development across all stages of discovery and development. Through early 2019, he was Senior Director in AbbVie’s drug product R&D organization, where he held a number of roles including head of preformulation, solid-oral formulation development, drug/device combination product development and CMC program management. In these roles, he was responsible for CMC technical strategy and execution for small molecule programs and combination product programs for biologics. Prior to AbbVie, John held similar scientific and leadership positions in Pharmaceutical R&D in Upjohn/Pharmacia/Pfizer. John founded FarmCMC LLC in 2019 to leverage his technical and leadership expertise to help small and medium sized biopharmaceutical companies develop novel therapeutic assets and delivery systems through early and late stage development. John received a Ph.D. in Analytical Chemistry from Purdue University, has more than 20 publications and presentations, and has served in various capacities with the American Association of Pharmaceutical Scientists, the Combination Product Coalition, and the IQ Consortium, where he was recognized with the Outstanding Service award in 2015.

engineered anitbodies, drug discovery, combination drug-device products, New modalities, mAbs, ADC, Bites, CAR-T, DVD, Dualbodies, mRNA, Molecular assessment and preformulation, Monoclonal antibodies, Multi-attribute Method (MAM), Biotherapeutics, Therapeutic Antibody Discovery, Bispecfic Antibodies, Combination Drug product, Protein Therapeutics, Screening Excipients

PNB - Medizinische Chemie, Pharmazeutische Chemie MQP - Pharmazie, Apotheke

235 mm

15.5 cm