Events

Filter by

Past events (2972)


EMA is initiating a new pilot programme for the expert panels to support manufacturers manufacturing and notified bodies certifying orphan medical devices with the challenges linked to generating clinical evidence for these devices in the premarket phase.

Event Human Rare diseases Medical devices

This is a hands-on training that covers user management, clinical trial life cycle, modifications, and responding to RFIs. Featuring a blended learning approach with on-demand, self-paced, and live virtual sessions.

Event Human Clinical trials
Event

The Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) was established under Regulation 2022/123 on a reinforced role for the European Medicines Agency in crisis preparedness and management for medicinal products and medical devices.

Event Human Veterinary Medicine shortages
Event Corporate

The Clinical Trials Coordination Group (CTCG), supported by the ACT EU Priority Action on Mapping and Governance, invites all stakeholders to the Clinical Trials Regulation (CTR) Collaborate Stakeholder Meeting.

Event Human Clinical trials