People (List)
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Biswarup Dasgupta
Biswarup Dasgupta (Bis) is a Quality and Compliance leader with experience in QA, and QC including contamination control over 23 years in the Biotech / Pharma Industries. -
Rich Davis
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Véronique D. Davoust, PharmD
Véronique Davoust has over 20 years experience in the pharmaceutical industry, both in Regulatory Affairs and Manufacturing, for Pfizer Inc. In her current position she is responsible for the monitoring and analysis of global and European emerging regulations and guidelines that impact manufacturing sites, especially focusing on Good Manufacturing and Distribution Practices, security of the supply chain, product shortages, serialisation and registration of the Quality section of Marketing Authorization dossier throughout the product life cycle. -
Maxwell De Long
Roche-Genentech
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Fabio De Martino
Global Head Quality Strategy & Business Operations, Kite Pharma
Fabio De Martino is currently Associate Director of Finance and Information Management Process Improvement at BioMarin Pharmaceutical. In this role, his main responsibilities are identifying, launching, leading and delivering critical projects, across all company functions, with significant tangible monetary impacts. -
Richard Denk, Skan AG
SKAN AG
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Michelle Dennis
MilliporeSigma
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Phil DeSantis
Phil DeSantis is a pharmaceutical consultant, specializing in Pharmaceutical Engineering and Compliance. He focuses on standards and practices for capital projects, facility and equipment-related site operations, sterilization and contamination control, and process validation. -
Rebecca A. Devine, PhD
Rebecca (Becky) Devine, PhD is an independent regulatory consultant with over 30 years of experience in the regulation of biological products. -
Mark Dickson
CSL Behring
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Lori Dingledine
Spark Therapeutics
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Danielle DiTirro
PhD
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Dr. Nickett Donaldson-Kabwe
Northern RNA Inc.
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Sumin Dong
Program & Project Manager, Genentech
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Susan Dounce
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Robert Dream
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Derek Duncan, PhD
Dr. Derek Duncan began his career as a Research Scientist at the Dutch Institute for Atomic & Molecular Physics in Amsterdam. He then moved into industry holding various Product & Application Development positions. Currently at LIGHTHOUSE and based in Amsterdam since 2003, Dr. Duncan is responsible for developing applications for pharmaceutical process monitoring and finished product inspection. These include using headspace analysis for container closure integrity testing, lyo chamber moisture mapping, and automated media fill inspection. Dr. Duncan has been a PDA member since 2004 and has been a regular contributor to PDA conferences, IG Groups, and Conference Program Committees. -
Eiji Watanabe
Eiji Watanabe worked for Terumo for 44 years and retired last year. He has been involved in the laboratory for many years in the design of infusions, syringes, topical formulation, peritoneal dialysis solutions, and product development of combination products. Currently, he uses his experience as a consultant. -
Walid El Azab
STERIS
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Ahmed Elsaid, Emergent Biosolution