Osamu Takahashi

  • Joined Nippon Mining (now ENEOS) in 1987, where he was involved in setting up the GMP system for investigational new drugs and developing manufacturing methods for chemically synthesized APIs.
  • Since 2002, worked in the quality assurance departments of Sumitomo Pharmaceuticals (now Dainippon Sumitomo Pharma), Mochida Pharmaceuticals, and Novartis Pharma, where he was in charge of GQP operations including quality audits.
  • He joined CM-Plus in September 2013 and obtained his auditor certification from the Committee of Active Pharmaceutical Ingredients of the European Federation of Chemical Industry in April 2014.
  • As a senior GMP consultant, he provides GAP analysis, inspection support, and Suppliers Audit in Japan and overseas, and also holds Auditor training seminars to support customer education. He also conducts GMP seminars in Japan and overseas.

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