Medical Devices Newsletter No. 29 - August 2010
30 August 2010
Content
- Editorial
- Changes to the Medical Devices Legislation that Impact Custom-made Medical Device Manufacturers
- New Approach and the IMB Post Market Surveillance Plan
- SCENIHR's Report on the Safety of Reprocessing Single-Use Medical Devices
- Regulatory Update
- Changes to MEDDEV 2.4/1 on the Classification of Medical Devices
- European Commission Public Consultation on the Revision of the In Vitro Diagnostic Medical Devices Directive (98/79/EC)
Medical Devices Newsletter No. 29 - August 2010