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ENATRANS Webinar - The regulation Ecosystem for Nanomedicine

ENATRANS organised this webinar on 1st december 2017 to inform about the regulation Ecosystem for Nanomedicine and to give practical advice about what is required and who can help at the different steps of the Nanomedicine regulation process. Recording of the webinar is available on YouTube.

ENATRANS Webinar - The regulation Ecosystem for Nanomedicine

ENATRANS organised this webinar on 1st December 2017 to inform about the regulation Ecosystem for Nanomedicine and to give practical advice about what is required and who can help at the different steps of the Nanomedicine regulation process. Recording of the webinar is available on YouTube: https://youtu.be/x__fGNRxmTA

 

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 gave 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 serve as a guide about what is required in which order and who can help at the different steps of the process.