An introduction to the regulatory approval challenges and guidances to help people working in the combination product regulatory environment
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It was a pleasure to attend the DIA Europe 2019 in Vienna - an event dedicated to bringing health care product development professionals together.
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The Chinese market is large, diverse and full of opportunities - but it can also be a challenging one. We guide you through the regulatory process of pharmaceutical drugs and medical devices in China.
China Regulatory Affairs
Michor Consulting were enjoying a breathtaking view of the city of Vienna while hiking through the Viennese vineyards in beautiful Indian Summer like weather. A great hike, combined with the culinary delights of the traditional Viennese Heuriger made this company trip a real adventure.
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Officers from the Hunan Provincial Food & Drug Administration paid a visit at Michor Consulting in Vienna in order to discuss
the regulation of medical devices on R&D, the registration regulation in Austria/EU,
the incentive system and the management system for devices manufacturers
and the importation of medical devices from the EU into the Chinese health care market.
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Michor Consulting were presenting their services at the BioPharma Expo 2018, Japan's largest exhibition for biopharmaceutical technologies, in Tokyo, Japan.
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Dr. Salma Michor, Dr. Franz Hofer and Dr. Alireza Hosseini, Vice President of CinnaGen, at the European Medicines Agency (EMA) in London, UK.
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Dr. Salma Michor and Dr. Franz Hofer gave an insight into Global Biosimilars and the characterization of Biosimilars at CinnaGen's "I like the new me" Stand Alone in Istanbul, Turkey.
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