Statement on agency’s efforts to increase transparency in medical device reporting
Posts published in June 2019
Personalized Medical Devices – Regulatory Pathways
Guidance on Therapeutic Goods (Conformity Assessment Standard for Quality Management Systems) Order 2019
12th Meeting of the Working Group on Guidelines on benefit – risk assessment of Phthalates in Medical Devices
Another Notified Body Bows Out Ahead of EU MDR: ‘Investment Too High’
Health Canada launches consultations to improve the safety of medical devices
Factsheet for healthcare professionals and health institutions
Mouse Embryo Assay for Assisted Reproduction Technology Devices
Update from the EU Council – Public session (health) – Friday, 14 June 2019 10:25 CET
UK NB Will Not Apply for EU MDR/IVDR