MHRA Medicines and Healthcare products Regulatory Agency Device Registrations – Reference Guide
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- COMMISSION IMPLEMENTING REGULATION (EU) 2026/977, of 4 May 2026, laying down certain uniform quality management and procedural requirements for the conformity assessment activities carried out by a notified body designated under Regulations (EU) 2017/745 and (EU) 2017/746 of the European Parliament and of the Council
- MASTER COURSE SUPLEMENTOS ALIMENTARES : “Evento muito bem organizado, conduzido e menistrado “
- Guidelines on the best practices for the traceability of medicines in hospital settings
- MDCG 2021-12 Rev.2 FAQ on the European Medical Device Nomenclature (EMDN) Revision 2 – April 2026
- GUIDELINE ON REQUIREMENTS FOR REVISION/RENEWAL OF CERTIFICATES OF SUITABILITY TO THE EUROPEAN PHARMACOPOEIA MONOGRAPHS
- EMA Clinical Data Publication (CDP)
- PLANOS DE CONTINGÊNCIA em Farmacovigilância: “Excelente formação, muito prática”
- Formação CTD MODULO 3 : ” Formação útil, clara e objetiva. Bons exemplos práticos para consolidar os conceitos abordados “