Marian Glynn, PhD, RAC, DABT
President and Principal Consultant
-
United States
Pharmaceuticals
Pharmacokinetics, Regulatory Requirements, Drug Development, Toxicology, CRO, Regulatory Submissions, Pharmaceutical Industry, Regulatory Affairs, GLP, Biopharmaceuticals, Drug Discovery
Experience
President and Principal Consultant
Tox Clarity, LLC
San Francisco Bay Area, California, United States
Regulatory strategy for efficient nonclinical development of novel medicines to best ensure go/no-go decisions are logical, regulators understand benefit/risk, and patients are informed. Progressing your program with focused nonclinical development strategies, rational regulatory science, and discerning due diligence.
Director, Preclinical and Translational Sciences
Takeda Pharmaceuticals
Cambridge, Massachusetts, United States
Director, Nonclinical Safety Evaluation
Sangamo Therapeutics, Inc.
Richmond, California, United States
Consulting Toxicologist and Preclinical/Nonclinical Regulatory Strategist
Tox Clarity, LLC
San Francisco Bay Area, California, United States
Toxicologist I-III
Dow Pharmaceutical Sciences, Inc. (now integrated into Bausch Health R&D)
Petaluma, California, United States
Marian Glynn, PhD, RAC, DABT's Contact Information
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