Anna Kaufman

Director of Regulatory Affairs



Anna Kaufman has 25 years of progressive pharmaceutical industry experience, including 10 years of analytical chemistry, followed by 15 years in regulatory affairs. She worked for Teva Pharmaceuticals, URL / Mutual Pharmaceutical Company, Sandoz and Qualitest / Par (Endo Health Solutions).



Anna has great experience in preparation of the regulatory submissions, including ANDAs NDAs (505 B2), INDs, briefing packages, post approval supplements, etc. for complex pharmaceutical dosage forms, including modified release solid dosage forms, suppositories, suspensions, sterile solutions and lyophilized products.


Anna brings a valuable understanding of the generic pharmaceutical industry and regulatory field in particular.


Anna holds an Engineering degree in Electrochemical Production from the Chemical Technology University in Moscow.  She joined Jubilant Cadista in August 2016.