荷兰
荷兰的醫療器械市場情報。覆蓋法規變化、競品動態和採購趨勢。
国家汇总表上次刷新：2026年8月7日（可能滞后）。上图「近 7 日」为实时重算。表内旧值 45。
近 7 日信號
Draft guideline on the requirements for demonstrating therapeutic equivalence for nasal products
Clinical trial applications advice pilot becomes permanent
Quality, preclinical and clinical aspects of gene therapy medicinal products - Scientific guideline - European Medicines Agency (EMA)
Physical frailty: instruments for baseline characterisation of older populations in clinical trials - Scientific guideline - European Medicines Agency (EMA)
Medical devices legislation - European Medicines Agency (EMA)
Concept paper on the guideline revision on good pharmacogenomic practice
Clinical investigation of medicinal products in the treatment of chronic obstructive pulmonary disease (COPD) - Scientific guideline - European Medicines Agency (EMA)
ICH M11 guideline, clinical study protocol template and technical specifications - Scientific guideline - ema.europa.eu
EMA Public Declaration of Interests form - European Medicines Agency (EMA)
Clinical investigation of medicinal products in the treatment of lipid disorders - Scientific guideline - European Medicines Agency (EMA)
Expert decision and opinion in the context of the Clinical Evaluation Consultation Procedure (CECP) - European Medicines Agency (EMA)
Clinical evaluation of new vaccines - Scientific guideline - European Medicines Agency (EMA)
Non-clinical requirements for radiopharmaceuticals - Scientific guideline - European Medicines Agency (EMA)
Guideline on quality, non-clinical and clinical requirements for investigational advanced therapy medicinal products in clinical trials - Scientific guideline - European Medicines Agency (EMA)
Clinical development of fixed combination medicinal products - Scientific guideline - European Medicines Agency (EMA)
ICH E6 Good clinical practice - Scientific guideline - European Medicines Agency (EMA)
Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 28 September - 1 October