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Consult GmbH & Co. KG
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Experts on
Good Clinical Practice
since 1993
Good Clinical Practice
since 1993
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More than 20 years of experience in pharmaceutical industry
- Organisation and management of several medical departments
- Management of a registration department
- Planning, management and evaluation of clinical trials and Post Marketing Surveillance (PMS/NIS), experience for more than 20 years
- Evaluation and management of basic research projects
- Establishing of different training manuals and training of monitors, investigators and pharmaceutical representatives
- Organisation of scientific symposia
- Evaluation of clinical papers and documents for acquisition of a product (indication, portfolio)
- Medical writing (PSUR, DSUR, SmPC, PIL)
- Meetings and discussions with regulatory authorities in Germany, Lithuania, Bahrain and Oman
- 15 years pharmacovigilance officer in Germany
- Several years pharmacovigilance officer for Austria and Switzerland, for Western Europe, Middle East and Far East
- 2 years safety officer for medical devices in Germany