EU Regulatory Resources

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 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 [...]

By |2021-10-07T18:41:06-04:00October 7th, 2021|EU Regulatory Resources|0 Comments

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 [...]

By |2021-10-01T14:41:28-04:00September 25th, 2021|EU Regulatory Resources, In the Press|0 Comments

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 [...]