Post-market surveillance as a medical device requirement in the EU

Don’t Have a Coronary... make the EU Regulatory Process work for you! (Cardiovascular Devices)Подробнее

Don’t Have a Coronary... make the EU Regulatory Process work for you! (Cardiovascular Devices)

Medical Device News November 2024 Regulatory UpdateПодробнее

Medical Device News November 2024 Regulatory Update

Information session on the pilot for expert panels' advice for orphan medical devicesПодробнее

Information session on the pilot for expert panels' advice for orphan medical devices

“Best Practices first Post Market Clinical Follow-Up(PMCF) Under EU MDR by Tim JalbotПодробнее

“Best Practices first Post Market Clinical Follow-Up(PMCF) Under EU MDR by Tim Jalbot

Understanding Post-Market Surveillance (PMS) for Medical DevicesПодробнее

Understanding Post-Market Surveillance (PMS) for Medical Devices

Understanding Compliance - U.S. FDA and EU MDRПодробнее

Understanding Compliance - U.S. FDA and EU MDR

EU MDR Hot Takes: Evolution or Overreach?Подробнее

EU MDR Hot Takes: Evolution or Overreach?

SYS-019 Post-market Surveillance Procedure WebinarПодробнее

SYS-019 Post-market Surveillance Procedure Webinar

Navigating the Red Tape - Discussing Regulatory updates for MedTech in the United KingdomПодробнее

Navigating the Red Tape - Discussing Regulatory updates for MedTech in the United Kingdom

Monitoring safety of Drug-Device CombinationПодробнее

Monitoring safety of Drug-Device Combination

Understanding Post-market Surveillance under EU MDR: Being Proactive, not ReactiveПодробнее

Understanding Post-market Surveillance under EU MDR: Being Proactive, not Reactive

AI Act in Medical Device Industry & Europe - Key Objectives & What you need to know.Подробнее

AI Act in Medical Device Industry & Europe - Key Objectives & What you need to know.

Launch Medical Device to Market in the EU vs USПодробнее

Launch Medical Device to Market in the EU vs US

How to do Postmarketing Surveillance the right way?Подробнее

How to do Postmarketing Surveillance the right way?

EU Medical Device Regulations and ComplianceПодробнее

EU Medical Device Regulations and Compliance

Webinar: Mastering Medical Device Regulations (EU) 2017/745 - Integration and Compliance GuidanceПодробнее

Webinar: Mastering Medical Device Regulations (EU) 2017/745 - Integration and Compliance Guidance

Clinical and Post Market Surveillance Requirements under the MDRПодробнее

Clinical and Post Market Surveillance Requirements under the MDR

Prepping your QMS for EU MDRПодробнее

Prepping your QMS for EU MDR

Post-Market Surveillance for Medical Devices & Combination ProductsПодробнее

Post-Market Surveillance for Medical Devices & Combination Products

Webinar: Post-marketing safety surveillance of medical devices and DDC products, EU and USAПодробнее

Webinar: Post-marketing safety surveillance of medical devices and DDC products, EU and USA