MDR Clinical Evaluation Reports: Key Elements and Lessons Learned for Successful Compliance
Access On-Demand Webinar Here.
As the MDR mandatory implementation date approaches, several manufacturers continue to question their preparedness for compliance. To date, NAMSA has supported numerous clients through MDR transitions and as a result, has gained unique perspectives from these projects, including Notified Body feedback.
NAMSA invites you to join us for this webinar, which will include a panel discussion with our medical writing experts. Attendees will walk away with unique solutions and strategies for successful MDR planning to meet the May 25, 2021 conformity date.
Highlighted will be discussion on:
- Insights and lessons learned from real-world client and Notified Body experiences
- How to expertly apply requirements for Clinical Evaluation Reports (CERs)
- Helpful considerations as the medical device industry approaches MDR deadlines
There will also be an opportunity to address the panel in a Q&A session during the last 15 minutes of the webinar. If you have a topic or question you would like to submit prior to the webinar, you can do so by contacting us at communications@namsa.com.
*By registering for this event, you are providing NAMSA consent to contact you directly regarding NAMSA’s services. The information you are providing will be processed by NAMSA to better understand your product needs and interests. At any time, you can submit a request to withdraw your consent for the use of information provided by you by contacting us at: communications@namsa.com. For additional information, please visit our Privacy Policy or contact us at privacy@namsa.com.
NAMSA uses a third-party provider, GoToWebcast, to host NAMSA webinars. For information related to GoToWebcast’s privacy policy and utilization of information, please contact GoToWebcast directly.