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Fiona Sibley is a senior regulatory affairs consultant with CTD Quality Consulting, with 18 of years experience in the Biotechnology and pharmaceutical industry, including 11 years in regulatory Affairs.
Having worked for Biogen for 11 years, Fiona's regulatory experience spans all phases of drug development, from pre-clinical to post-marketing. For the past 7 years, Fiona has worked as a consultant with biologics and drugs specializing in Chemistry, Manufacturing and Controls (CMC) and related submissions.
Her Clients include Genetics Institute, Wyeth, Boston Scientific, Biogen-idec, Millenium Pharmaceuticals, Guidant, Therion and a number of small companies.
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