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Registration types and regulatory requirements for the Asia Pacific region

The English-speaking seminar “Registration types and regulatory requirements for the Asia Pacific region” qualifies you to improve approvals for the Asia pacific markets. It provides you the framework condition as well as regulatory requirements for a successful approval of medical devices.

  • Registration of medical devices in Australia: Therapeutic Goods Administration (TGA), Medical Device Single Audit Program (MDSAP) requirements, Australian Regulatory Guidelines for Medical Devices (ARGMD), Australian Register of Therapeutic Goods (ARTG)
  • Registration of medical devices in Korea: Ministry of Food and Drug Safety (MFDS, formerly known as KFDA), Medical Device Act (MDA), Korean Good Manufacturing Practice (KGMP)
  • Registration of medical devices in Japan: Pharmaceutical and Medical Device Act (PMD Act), Ministry of Health, Labour and Welfare (MHLW), Pharmaceuticals and Medical Devices Agency (PMDA)
  • Registration of medical devices in Taiwan: Taiwan Food and Drug Administration (TFDA), Pharmaceutical Affairs Act, Regulations for Governing the Management of Medical Device, Regulation for Registration of Medical Device
  • Registration of medical devices in Malaysia: Medical Device Act (MDA), Medical Device Authority Act (MDAA), ASEAN Medical Device Directive (AMDD)
  • Registration of medical devices in Singapore: Health Science Authority (HAS), Medical Device Information and Communication System (MEDICS), AMDD
  • Registration of medical devices in China: legal framework of the NMPA, Classification of Medical Devices according to NMPA and Registration Partition, Registration Type, Approval Process of Medical Devices and Post-Market Surveillance
Target Group
  • Medical Device Manufacturers
  • Newcomers in the medical device industry
  • Expert and executive personnel that want to update their knowledge
  • Personnel in charge of regulatory affairs
  • Personnel in quality management
  • Engineers in the medical device industry
  • Consultants in the medical device industry
  • Medical Safety Officer‘s
Training Goal

Within the scope of regulatory affairs, you can take responsibility for the global registration of your medical devices and basic understanding of the regulations helps you to register your devices in the APAC-region.

Services

The participation fee includes the seminar documents, meals and the participation certificate. Of course, there will also be an opportunity to exchange experiences with the participants and to discuss with our experts.

Booking

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