[Webinar]How Innovation Empowers Companies in a Complex Regulatory Landscape
The medical device industry is heavily regulated, facing complex data requirements established by European Union (EU) regulations such as the EU Medical Device Regulation (MDR); the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) Regulation; and the Restriction of Hazardous Substances (RoHS) Directive.
Medical device companies must evaluate a large volume of supplier data to determine which markets a product can be sold in. The industry leverages standardized data exchange formats such as IPC-1752A to manage these requirements. Standardization allows for the development of innovative technologies to streamline data validation and remove bias from the evaluation of supplier documentation.
Register for the Webinar Today!
9AM ET | 6AM PT | 1PM GMT
Thursday, May 7, 2020
Approximately 60 minutes
In this presentation by Travis Miller, Assent’s General Counsel, and David Strutt, Assent’s Senior Product Manager, attendees will:
Learn about key industry requirements, including Section 10.4 of the EU MDR, that complicate supply chain data acquisition and assessment.
Understand how the industry is responding to supply chain data requirements through standardization, process and technology.
Learn how Assent’s innovative technologies dramatically reduce document review time and increase both data accuracy and consistency.
During the presentation, you will see how Assent’s software capabilities enable medical device companies to meet their strict requirements more efficiently and effectively within an environment that is rapidly growing in complexity.