
Christopher Fredric
A very experienced Regulatory Affairs executive in the biotech/pharmaceutical industry. Significant accomplishments in designing and implementing Regulatory... | Sanofi, 195 Merton St, Canada
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Christopher Fredric’s Emails cf****@ca****.com
Christopher Fredric’s Phone Numbers 1647436****
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Christopher Fredric’s Location Sanofi, 195 Merton St, Canada
Christopher Fredric’s Expertise A very experienced Regulatory Affairs executive in the biotech/pharmaceutical industry. Significant accomplishments in designing and implementing Regulatory strategies in the filing and approval of drugs developed for rare diseases. Extensive experience in leading regulatory teams to prepare, file marketing authorizations and support the application through licensure & post approval process with FDA, EMA, Health Canada, Middle-East, North Africa, Israel, Asia, Latin America and other international regulatory agencies. - A strategic thinker, proactive with a global perspective and goal oriented - Proven track record of success. Brings a wealth of knowledge in pharmaceutical product development - Excellent project management and organizational skills - Experience in pharmacovigilance activities for marketed products, product launch submissions including Advertisement, Promotional Labeling, and patent searches - Identifies, selects and engages high-performing teams - In-depth understanding of biotech business - Vast knowledge of ICH Guidelines, GMP, GCP and GLP including international regulatory requirements for clinical development programs
Christopher Fredric’s Current Industry Sanofi
Christopher
Fredric’s Prior Industry
Advanced Biological Products
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Sanofi Pasteur
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Cobalt Pharmaceuticals
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Emergent Biosolutions
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Seneca College
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Covalon Technologies
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Alexion Pharmaceuticals
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Optuminsight
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Nono
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Sanofi
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Work Experience

Sanofi
Director, Global Regulatory Affairs Leader (Transplant)
Sat Jan 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Covalon Technologies
Senior Director, Regulatory Affairs
Sat Jun 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Jan 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time)
Nono
Executive Director, Scientific Affairs
Thu Mar 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed May 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time)
Alexion Pharmaceuticals
Associate Director, Regulatory Affairs
Tue Jan 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Jan 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time)
Optuminsight
Associate Director, US Regulatory Affairs
Tue Jan 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Jan 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time)
Covalon Technologies
Manager, Clinical and Regulatory Affairs
Sun Jan 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Jan 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time)
Seneca College
Professor, Continuing Education. Pharmaceutical Regulatory Affairs and Quality Operations Program
Mon Jan 01 2007 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Jan 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time)
Emergent Biosolutions
Manager, Regulatory Affairs
Thu Jan 01 2004 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Jan 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time)
Cobalt Pharmaceuticals
Senior Regulatory Affairs Associate
Tue Jan 01 2002 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Jan 01 2004 00:00:00 GMT+0000 (Coordinated Universal Time)
Sanofi Pasteur
RA Associate
Mon Jan 01 2001 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Nov 01 2002 00:00:00 GMT+0000 (Coordinated Universal Time)
Sanofi Pasteur
Research Technologist
Sun Jan 01 1995 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Jan 01 2001 00:00:00 GMT+0000 (Coordinated Universal Time)
Advanced Biological Products
Research Scientist-Part Time
Sat Jan 01 1994 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Jan 01 2001 00:00:00 GMT+0000 (Coordinated Universal Time)