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To enable companies to develop and execute innovative and successful regulatory strategies in the global arena of drug development across the entire lifecycle, are key deliverables of my work as a Consultant.
Consulting Services
My key deliverables of as a Consultant:
Enable companies to develop and execute innovative and successful regulatory strategies in the global arena of drug development across the entire lifecycle.
I have been responsible for the successful registration of 20+ innovative medical products and new indications (Biotech, low-molecular and Plasma products) in more than 50 countries.
Clients benefit from my experience across the entire product lifecycle, including orphan drug development, from early development to approval & launch in various therapeutical areas, including oncology, hematology, immunology, and, CV, CNS and metabolic diseases.
Catarina Edfjäll PhD, Board Director, Mentor & Coach
Global Regulatory Affairs Expert
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