Ernst & Young new report on how the global medical technology (medtech) industry
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Recentes
- Article 10a MDR / IVDR: Notification in Case of Interruption or Discontinuation of Supply Decision Guide Flowchart
- New Qualification & Validation Guidelines for Pharma in 2025
- ENISA Cybersecurity Maturity & Criticality Assessment of NIS2 sectors
- EMA FAQs How to submit an annual safety report and respond to related RFIs
- Questions and answers on the Critical Medicines Act
- Atualização das listas previstas no regulamento sobre o controlo de transações de medicamentos para o exterior do país (março 2025)
- Factsheet – Critical Medicines Act: Improving the availability and securing supply of critical medicines in the EU
- Artificial Intelligence and Medical Products: How CBER, CDER, CDRH, and OCP are Working Together (March 2024, Revised February 2025);