Asia-Pacific-Requirements
Online
trainingcentergermany@nsf.org
- Kosten: 249,00 €
Nächster Termin28.11.2024
Start / Ende10:00 / 14:30
OrtOnline
Kostenab 249,00 €
Beschreibung
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 as well as regulatory requirements for a successful approval of medical devices.
The seminar covers the following topics:
Participation in an online training course can take place via PC, tablet or even smartphone. All that is required is an internet connection and a standard internet browser. No special software is required for participants. A headset is certainly helpful to suppress background noise. An integrated loudspeaker and microphone ensure an interactive exchange between the participants during the online seminar.
The participation fee includes the seminar documents in electronic form and a certificate of attendance. There will of course also be an opportunity for participants to share their experiences and discuss with our experts.
Our online seminars continue to offer you the opportunity to find out about current topics in medical technology.
During the live presentation on the Internet, you can of course communicate directly with our speakers. In order to optimise the transfer of knowledge, this online seminar is designed to last approx. 4.5 hours so that we have enough time for your comments and questions. Furthermore, a small group of participants guarantees an interesting exchange of experiences with each other and with the speaker.
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.
Asia-Pacific-Requirements
Asia-Pacific-Requirements
Asia-Pacific-Requirements