Dror Wohlfeiler

Areas of Expertise: Regulatory Affairs
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Dr. Wohlfeiler is a pharmaceutical professional with more 27 years of experience gained working in the EU, US, Israel, Japan and other Asian countries, in site, regional and corporate roles.
Currently working in various global pharmaceutical companies in Europe in different consultancy project; from FDA compliance readiness and lab management, to overseeing an analytical technology transfer to a Chinese CMO.
Heading the Japan specialty and generic R&D project development at Teva from 2007. Before 2007 acted as head of Quality Control for Teva’s operation division. Built and managed teams in Branded and Generic R&D, supervised global project teams for Phase I – III
drug developments resulting in more than 100 approved ANDA submissions, 1 NDA and numerous Phase 3 trials in Japan.

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