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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 for the medical device approval process in the Asia Pacific markets. It provides you the framework condition as well as regulatory requirements for a successful approval of medical devices.
The seminar will discuss the following topics:
- 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, Labor and Welfare (MHLW), Pharmaceuticals and Medical Devices Agency (PMDA), Medical Device Single Audit Program (MDSAP) requirements
- Registration of medical devices in Taiwan: Taiwan Food and Drug Administration (TFDA), Medical Device Act(2021-05-01), Regulations for Governing Issuance of Medical Device License, Listing and Annual Declaration, Post-market Surveillance in Taiwan
- Registration of medical devices in ASEAN countries (Malaysia, Singapore, Philippines, Thailand): Responsible Authorities, ASEAN Medical Device Directive (AMDD), ASEAN Common Submission Dossier Template (CSDT), Singapore’s regulatory framework
- Registration of medical devices in China: regulatory framework of China, Classification of Medical Devices according to NMPA and Registration Unit, Registration Type, Approval Process of Medical Devices, QMS Requirements 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 Officers
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.
Costs
890 € excl. tax
Buchung
Leider ist eine Buchung für dieses Seminar nicht mehr möglich. Bitte wählen Sie einen Alternativtermin.Verfügbare Termine: