FDA Regulatory Pathways and Programs

Global Regulatory Roundtable: FDA and Notified Body PerspectivesПодробнее

Qualifying Biomarkers to Support Rare Disease Regulatory Pathways: Afternoon SessionsПодробнее

FDA Regulatory Education for Industry (REdI) Annual Conference 2023 – Devices Day 1Подробнее

FDA Product Regulations Part 6 of 7Подробнее

IGRF Webinar: Regulatory Pathways for Software as Medical Device (SaMD)Подробнее

IGRF Webinar: Regulatory Pathways for Software as Medical DeviceПодробнее

Regulatory Pathway and Applications in Drug Development for Rare DiseasesПодробнее

FDA Regulation of Cardiovascular Medical DevicesПодробнее

Demystifying the FDA Regulatory Path and Profession for Medical Devices and SoftwareПодробнее

Software Thought Leadership Series - FDA REGULATION OF CLINICAL DECISION SUPPORT SOFTWARE AND AI/MLПодробнее

FDA Product Regulations Part 1 of 7Подробнее

LMSDR Webinar: FDA Oncology Product DevelopmentПодробнее

Regulatory Pathways to Clearance: Transitioning University DiscoveriesПодробнее

The Regulation of SaMD in the USПодробнее

Regulatory Best Practices for Global Access to Medicines Including Anti-TB Medicines Day 2-Session 1Подробнее

FDA Clinical Investigator Training Course (CITC) 2022, Day 1 – Part 1Подробнее

FDA Product Regulations Part 4 of 7Подробнее

Regulatory Affairs & Drug Development Course from US FDA || Free Online Course with CertificateПодробнее