This is a degraded experience of openRID. Please enable JavaScript and use an up to date browser.

Regulatory information for medical devices/in-vitro diagnostic medical devices

Latest updates

Search all documents

ZL000_00_014e_WL Guidance document Time limits for authorization applications

From Swiss Agency for Therapeutic Products (Swissmedic) 🇨🇭

June 1, 2024

ZL300_00_001e_WL Guidance document Variations and extensions HAM

From Swiss Agency for Therapeutic Products (Swissmedic) 🇨🇭

June 1, 2024

ZL105_00_003e_WL Guidance document Meeting for applicants held with the Authorisation sector

From Swiss Agency for Therapeutic Products (Swissmedic) 🇨🇭

June 1, 2024

Important annual charge deadlines

From Therapeutic Goods Administration (TGA) 🇦🇺

May 31, 2024

Custom-made medical devices

From Therapeutic Goods Administration (TGA) 🇦🇺

May 31, 2024

Medical Device Policy News

From Ministry of Food and Drug Safety (MFDS) 🇰🇷

May 31, 2024

Announcements

From Ministry of Food and Drug Safety (MFDS) 🇰🇷

May 31, 2024

Public Inspection: Statement of Organization, Functions, and Delegations of Authority

From Food and Drug Administration (FDA) 🇺🇸

May 30, 2024

Infringement notices

From Therapeutic Goods Administration (TGA) 🇦🇺

May 30, 2024

Personal Protective Equipment (PPE)

From Therapeutic Goods Administration (TGA) 🇦🇺

May 29, 2024

Investigator’s brochures for medical device clinical trials

From Therapeutic Goods Administration (TGA) 🇦🇺

May 29, 2024

Guidance on Personal Protective Equipment: health professionals

From Therapeutic Goods Administration (TGA) 🇦🇺

May 29, 2024

Safety announcements from medical device manufacturers

From Danish Medicines Agency (DKMA) 🇩🇰

May 31, 2024

Safety information

From National Agency for the Safety of Medicines and Health Products (ANSM) 🇫🇷

May 31, 2024

Recalls and safety alerts

From Health Canada 🇨🇦

May 31, 2024

List of recalls and other field safety corrective actions (FSCA)

From Swiss Agency for Therapeutic Products (Swissmedic) 🇨🇭

May 31, 2024

Safety Alerts on Medical Devices

From Ministry of Health (Italy) (MDS) 🇮🇹

May 31, 2024

Medical Device Recalls

From Food and Drug Administration (FDA) 🇺🇸

May 30, 2024

Recalls of medical devices

From National Organization for Medicines (EOF) 🇬🇷

May 28, 2024

Alerts

From Brazilian Health Regulatory Agency (Anvisa) 🇧🇷

May 28, 2024

Weekly reports of the National Center for Medical Devices and Products Reporting

From Saudi Food and Drug Authority (SFDA) 🇸🇦

May 26, 2024

Product Recalls

From National Medical Products Administration (NMPA) 🇨🇳

May 24, 2024

Alerts and recalls of medical products - ANMAT

From National Administration of Drugs, Food and Medical Devices (ANMAT) 🇦🇷

May 14, 2024

Medical Devices Safety Notices

From Health Products Regulatory Authority (HPRA) 🇮🇪

May 13, 2024

openRID is

34

Organizations

4,885

Datasets

15,412

Files