Netherlands
Intelligence de marché des dispositifs médicaux pour Netherlands. Changements réglementaires, concurrents et tendances d'achats.
Table pays dernière MAJ : 7 août 2026 (peut être en retard). Le total 7 j est recalculé en direct (ancienne valeur table : 45).
Signaux des 7 derniers jours
eAF Release Notes v1.25.0.0 - EMA eSubmission
Hemoblast - European Medicines Agency (EMA)
EMA Public Declaration of Interests form - European Medicines Agency (EMA)
EMA Public Declaration of Interests form - European Medicines Agency (EMA)
Qualification of novel methodologies (QoNM) for medicinal product development_Procedural Guidance for applicants - European Medicines Agency (EMA)
EMA Public Declaration of Interests form - European Medicines Agency (EMA)
Guideline on the content, management and archiving of the clinical trial master file - European Medicines Agency (EMA)
EMA Public Declaration of Interests form - European Medicines Agency (EMA)
Overview of comments on the draft guideline on quality requirements for drug-device combinations (EMA/CHMP/QWP/BWP/259165/2019) - European Medicines Agency (EMA)
ICH E3 Structure and content of clinical study reports - Scientific guideline - European Medicines Agency (EMA)
Clinical development of medicinal products intended for the treatment of pain - Scientific guideline - European Medicines Agency (EMA)
Clinical investigation of human normal immunoglobulin for subcutaneous and/or intramuscular administration (SCIg/IMIg) - Scientific guideline - European Medicines Agency (EMA)
EMA Public Declaration of Interests form - European Medicines Agency (EMA)
Clinical investigation of medicinal products for treatment of rheumatoid arthritis - Scientific guideline - European Medicines Agency (EMA)
Overview of comments received on draft guideline on the development of medicinal substances contained in drug-eluting (medicinal - European Medicines Agency (EMA)
Voluntary data submission pilot to advance innovative alternatives to animal testing
EMA Public Declaration of Interests form - European Medicines Agency (EMA)
Guide to manufacturers and notified bodies on the procedure for requesting advice from expert panels for orphan medical devices | European Medicines Agency - European Medicines Agency (EMA)