European Commission’s Call for Evidence for an Impact Assessment: Sustainable Consumption of Goods – Promoting Repair and Reuse
The Association of Medical Device Reprocessors (AMDR) represents the worldwide interests of commercial [...]
AMDR comments to the UK Medicines and Healthcare Products Agency (MHRA)
. . . AMDR does not believe the additional specific requirements outlined in [...]
AMDR comments to the Autoridade Nacional do Medicamento e Produtos de Saúde I.P.
AMDR appreciates Infarmed’s decree clarifying Portuguese policy for reprocessing and remanufacturing of single-use [...]
Healthcare Without Harm: Measuring and Reducing Plastics in the Healthcare Sector
Plastic has become ubiquitous in healthcare, with a dramatic shift towards single-use items [...]
AMDR comments to the Spanish Royal Decree Regulating Medical Devices
The Association of Medical Device Reprocessors (AMDR) appreciates the opportunity to comment on [...]
Latvia: Changes in the legal landscape for medical devices in the Baltics – MDR/IVDR
As well as this, the draft regulations introduce the recycling and reuse of [...]
Legal Framework: Belgium
Belgium published guidelines for the remanufacturing of single use medical devices in January [...]
Legal Framework: Netherlands
The Netherlands published guidelines for the remanufacturing of single use medical devices in [...]
Legal Framework: Germany
The legal basis for reprocessing under German law (MP Betreiber V) changes on May 26 2021 [...]