Tuttlingen – Whether Argentina, Australia, Canada, Mexico, China, Japan, USA, Russia or Saudi Arabia: there are numerous promising markets for medical products. In order to raise their potential, the hurdle "approval procedure" must be cleared, which can be as different as the country itself. Support on this path will be provided by several seminars in autumn.
It no longer takes 80 days to circumnavigate the world. Five is enough between September and November to get to know and internalize the approval procedures of well-known and proven countries, but also of several "emerging markets" - which in a way is also like a trip around the world, because basically every country has medical technology "Made in Germany". Expression. Let's start with an Atlantic crossing. North America continues to play a key role in the export business, especially the USA. What FDA & Co have in terms of specifications will be explained on two consecutive days on September 22nd and 23rd. The participants cross the continent from north to south on October 19th: The admission journey runs from Canada via Mexico, Colombia and Brazil down to Argentina. If you want, you can book the connecting ticket across the Pacific directly - on November 11th, the focus will be on the legal regulations in Australia, Malaysia, Singapore, South Korea, Russia and Saudi Arabia. The Asian market in particular offers enormous opportunities for manufacturers - but it is not without risk. Therefore, on October 6th, world travelers will receive well-founded information on what needs to be considered in China, Japan and Taiwan when it comes to medical technology.
This year's seminars on international approval procedures in detail:
- Medical Device Approval Process in the USA (2 days)
22./23. September - Approval procedures for medical devices in China, Japan and Taiwan
October 6th - Approval procedures for medical devices in Brazil, Mexico, Argentina, Colombia and Canada
October 19th - Medical device approval processes in Malaysia, Singapore (ASEAN), Australia, South Korea, Russia and Saudi Arabia
November 11th
Knowledge of the EU MDR and DIN EN ISO 13485 is recommended.
