Mastering Compliance: Essential Insights into PMS Documentation – Webinar What: Webinar in partnership with Medtech Intelligence - “Mastering Compliance: Essential Insights into PMS Documentation” When: Wednesday, April 24th, 2024 | 10:00 am – 11:00 am EST Where: Online Event How: Register Here - this webinar will include a 45-minute presentation and 10
Strategies for Successful PMCF under EU MDR: Unlocking the Mystery – Webinar in partnership with Medtech Intelligence What: Webinar in coordination with Medtech Intelligence - “Strategies for Successful PMCF under EU MDR: Unlocking the Mystery” When: March 6th, 2024, 10:00 am – 11:00 am EST Where: Online Event How: Register Here -
Webinar: Navigating Clinical Evaluation Excellence: A Strategic Guide for Medical Devices What: Webinar - “Navigating Clinical Evaluation Excellence: A Strategic Guide for Medical Devices” When: Tuesday, December 5, 2023, 9:30 am Central US Time | 4:30 pm Central EU Time Where: Online Event How: Register Here Why: Join us in this insightful webinar as
Optimizing CER and PMS Document Writing with Technology and AI – Webinar in partnership with Medtech Intelligence What: Webinar in coordination with Medtech Intelligence examining the common non-conformities encountered during clinical evaluations and explore how technology can play a pivotal role in resolving these challenges. When: September 26th, 2023, 10:00 am – 11:00
Is the EU MDR Extension a Blessing or a Curse? What: Webinar - “Is the EU MDR extension a blessing or a curse?” When: Thursday, August 24th 2023, 10:00 – 11:00 ET Where: Online Event How: Register Here Why: Join this session to better understand the effects of the EU MDR extension on
Leveraging Technology to Optimize MDR Compliance Outsourcing and Partnership What: This is a webinar showcasing how our partnership with Acumed benefited from the usage of our CAPTIS solution. We will be discussing how medical device organizations can achieve efficiency, save time and improve accuracy by incorporating automation into their systematic literature review and
IVDR Survival Guide - Common Pitfalls Encountered in Complying with the Regulation's Requirements - Webinar What: Webinar - “IVDR Survival Guide - Common Pitfalls Encountered in Complying with the Regulation's Requirements” When: Thursday, April 27th 2023 at 9:30 AM CT Where: Online Event How: Register Here Why: Join our medical devices/IVD expert, Smridula Hariharan
Clinical Evaluation of Dental Medical Devices – Lessons Learned from Notified Body Assessments - Webinar What: Webinar and Panel Discussion – “Clinical Evaluation of Dental Medical Devices – Lessons Learned from Notified Body Assessments” When: Tuesday, February 28th, 2023, at 10 AM ET Where: Online Event How: Register Here Why: Join us to examine
Implementing and Maintaining PMS & Performance Evaluation under the IVDR – Webinar Q&A Celegence, a Global Regulatory Affairs Services & Technology company for the Life Sciences Industry, partnered with Q1 Productions in September 2022 to offer a webcast titled “Implementing and Maintaining PMS and Performance Evaluation under the IVDR”. By replaying this webinar,
Implementing and Maintaining PMS & Performance Evaluation under the IVDR – Webinar Replay James Shearn is Celegence’s Regulatory Affairs Subject Matter Expert for Medical Devices and IVDs. He has worked in the Medical Devices and In Vitro Diagnostic Devices (IVD) sector for 27 years. Webinar Background: The EU In Vitro Diagnostic Devices Regulation
