ENATRANS Webinar - The regulation Ecosystem for Nanomedicine
1 Decembre 2017 - 1 Decembre 2017
Germany
The translation of any new medical invention into a final product is a highly regulated and complex process. To bring a new medical product or device on the market it has to go through a long and complex process involving many authorities at regional, national and international level.To successfully manage this process it is mandatory to study and understand the different parts of the process in detail.
The webinar gives an overview of the broader nanomedicine ecosystem and issues to be aware of such as regulation, pricing and reimbursement systems by providing all data about these steps in place in Europe, at the EU, and Member States level. The provided information, links and downloads will serve as a guide about what is required in which order and who can help at the different steps of the process.
Free-of-charge registration at: https://zoom.us/meeting/register/8c53975e94f9846b34538d7d4481ef37(s’ouvre dans une nouvelle fenêtre)
The webinar gives an overview of the broader nanomedicine ecosystem and issues to be aware of such as regulation, pricing and reimbursement systems by providing all data about these steps in place in Europe, at the EU, and Member States level. The provided information, links and downloads will serve as a guide about what is required in which order and who can help at the different steps of the process.
Free-of-charge registration at: https://zoom.us/meeting/register/8c53975e94f9846b34538d7d4481ef37(s’ouvre dans une nouvelle fenêtre)
Mots‑clés
Nanomedicine, Nanobiomedical, regulation, translation, nanotechnology for healthcare