This article provides information on the correct procedure for reporting a notification procedure in accordance with Section 32 StrlSchG (Strahlenschutzgesetz (German Radiation Protection Act)) as part of CTR submission and for Substantial Modifications in CTIS.

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 25266/25

This report highlights two key milestones: the recent manual workshop in Tanzania and the first continental clinical assessment training – both of which underscore the fellowship's commitment to capacity-building and harmonization across the African continent.

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 25677/25

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 10321/24

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 20838/25

Product group Medical data processing (software) - others
Reference 19784/25

Product group Electromedical fields - equipment for MR tomography
Reference 25917/25

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 25681/25

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 24142/25

CHMP Meeting Highlights May 2025

CHMP Meeting Highlights June 2025

CHMP Meeting Highlights July 2025

Product group Medical data processing (software) - others
Reference 18718/25

Product group General equipment for medical treatment - ward equipment and equipment for emergency medical services
Reference 23855/25

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 20664/25

Product group Dental products - instruments
Reference 00458/25

Product group ophthalmological technology - contact lenses
Reference 19212/25

Product group Non-active implants - bone surgery
Reference 25095/25

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 24062/25