LDT vs IVD: Adapting to the New FDA Regulations - MCRA Webinar

The FDA’s Final Rule on LDTs: What You Need To KnowПодробнее

FDA Webinar: Regulatory Oversight of Laboratory Developed Tests LDTsПодробнее

Complying with the FDA’s Rule on LDTs – What you need to Do and WhenПодробнее

LDT VS IVD Practicum Component 1Подробнее

FDA's Final Rule on LDTs is here: An informational webinar on how it will impact your lab.Подробнее

IVD vs. RUO–Is Your Laboratory Relying on the Right Products?Подробнее

Upcoming revisions of EU regulations & the reclassification of In Vitro DiagnosticsПодробнее

A New Regulatory World for Laboratory-Developed TestsПодробнее

New Requirements for In Vitro Diagnostics: Lessons Learned from the AAMI/FDA/BSI Annual ConferenceПодробнее

Benchtop Performance Testing Webinar - Jan. 25, 2024Подробнее

Webinar: A Regulatory Q&A With IVD Expert Robyn MeurantПодробнее

Overview of the new EU- In-vitro Diagnostics regulation.Подробнее

Exploring Concerns Surrounding the VALID ActПодробнее

Advances in In Vitro Bioequivalence Assessment for Topical ProductsПодробнее

What Are LDTs and How Are They Regulated?Подробнее

Navigating the Global IVD LandscapeПодробнее