- Lançamento do Projeto-piloto de Submissão de Ensaios Clínicos
- Clinical Trials Information System (CTIS): EMA training programme
- IMDRF :Principles of In Vitro Diagnostic (IVD) Medical Devices Classification
- Adapting COVID-19 vaccines to SARS-CoV-2 variants: guidance for vaccine manufacturers
- CLINICAL TRIALS REGULATION:(EU) Nr. 536/2014.
- EMA has published the EU IDMP Implementation Guide version 2.0
- Guideline on good pharmacovigilance practices (GVP) 4 Module XVI – Risk minimisation measures: selection of tools and 5 effectiveness indicators (Rev 3)
- EUDAMED NEWS: management of legacy devices.