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Thursday, May 11th

Webinars

E-health technologies in Medical Devices: identification of the key development milestones and regulatory constraints

When developing E-healthcare technologies with the objective to market them in Europe, it is key to well understand the regulatory issues to launch a product on time on the market.

The objective of this webinar is to present how to implement a strategic development plan for e-healthcare solutions while taking regulatory requirements into account in order to minimize risk.

During this webinar, the following issues will be discussed:

Applicable regulatory environment
E-healthcare products’ Development and assessment
Main regulatory obstacles in Europe

E-health technologies in Medical Devices: identification of the key development milestones and regulatory constraints

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