Best Practices for UDI Implementation and EUDAMED Submissions

 Upcoming Webinar Best Practices for UDI Implementation and EUDAMED Submissions Wednesday, January 20, 2021| 9 AM CST This webinar will include a 45 minute presentation and 10 to 15 minutes of Q&A. If your 2021 distribution strategy involves marketing...

EU MDR IMPACT TO DRUG DEVICE COMBINATIONS AND DEVICE CLASSIFICATION

 Archived Webinar EU MDR Impact to Drug Device Combinations and Device Classification Jeremy Moore, Associate Director, Medical Device and Combination Product QualityAbbVie Recorded on December 9, 2020 EMA Guidance surrounding Article 117 and Drug-Device...

Case Study: Conducting Monitoring Visits Remotely for IVD Clinical Trials During the COVID-19 Pandemic

 Archived Webinar Case Study: Conducting Monitoring Visits Remotely for IVD Clinical Trials During the COVID-19 Pandemic Trish Landry, MBA, RAC, CCRP, Senior Vice President, Clinical OperationsBEAUFORT CRO Leah Hollins, MPH, BA, Senior Clinical Project...

Preparing Your Team for the EUDAMED Database

John N. Bradsher, PhD, RAC, Medical Device Regulatory Affairs & Quality Assurance Expert at Celegence will present a webinar: How to Start Preparing your RA/QA Team for the EUDAMED Databse on Tuesday, September 22 at 10 a.m. CST. Read on for John’s...

Considerations for IVD Involvement in the Emergency Use Authorization Pathway

 Archived Webinar Considerations for IVD Involvement in the Emergency Use Authorization Pathway Kelli Tanzella, Ph.D., Senior Director, Global Regulatory Affairs, Clinical & ComplianceLife Sciences SolutionsThermo Fisher Scientific November 4, 2020 Due to...