Hana

Dr. Danan has more than 20 years of experience in various aspects of pharmaceutical R&D from formulation and analytical development to regulatory compliance. She cofounded SITEC pharmabio in 2009 where she contributes to the management and to the development of the company.

In Europe she established her own consulting firms collaborating with pharmaceutical and biotech companies. Prior to that, she gained significant industrial experience working in product development divisions at Parke-Davis/Warner-Lambert (now Pfizer, USA) and Sola-Barnes Hind (USA). There, she acquired hands-on expertise in developing liquid, semi-solid and solid dosage forms and in the areas of analytical development and validation.

Hana holds a Ph.D. in Pharmaceutics and Pharmaceutical Analysis from University of Kentucky (USA) where she also worked on her post doctoral-studies, and a B.Sc. degree in Pharmacy from Damascus University (Syria).