EU Regulatory Resources

European Commission’s Medical Device Sector, Reprocessing of Single-Use Devices Page

‘Reprocessing’ refers to a process carried out on a used device in order [...]

By |2021-02-12T16:58:37-05:00February 12th, 2021|EU Regulatory Resources|Comments Off on European Commission’s Medical Device Sector, Reprocessing of Single-Use Devices Page

AMDR Reaction to Swedish Socialstyrelsen Report: Prerequisites for Reprocessing and Reusing Disposable medical Devices in Sweden

The Association of Medical Device Reprocessors (AMDR) applauds the Swedish National Board of [...]

By |2021-02-03T09:29:09-05:00February 3rd, 2021|AMDR-Generated Resource, EU Regulatory Resources, Global Regulatory Resource, Press Releases|Comments Off on AMDR Reaction to Swedish Socialstyrelsen Report: Prerequisites for Reprocessing and Reusing Disposable medical Devices in Sweden

AMDR Comments to the European Commission’s Inception Impact Assessment on the Sustainable Products Initiative

The Association of Medical Device Reprocessors (AMDR) appreciates the Commission’s efforts to promote [...]

By |2020-12-09T15:39:35-05:00November 16th, 2020|Blog, EU Regulatory Resources|Comments Off on AMDR Comments to the European Commission’s Inception Impact Assessment on the Sustainable Products Initiative

United Nations Development Programme: Sustainable Health Procurement Guidance Note

To have an impact on planetary health requires bold vision, direction, leadership and [...]

By |2021-01-14T20:24:55-05:00August 4th, 2020|EU Regulatory Resources, Global Regulatory Resource|Comments Off on United Nations Development Programme: Sustainable Health Procurement Guidance Note