From the Europa website the following press release was issued on 2 Feb 2012. The complete press release is below. The original press release may be viewed too. European Commission – Press release Medical devices: European Commission asks for further
1 Step Closer to EU Medical Device e-Labeling
Per Eucomed’s 7 October 2011 newsletter electronic labeling of medical devices (MDD & AIMDD) has been approved as a draft regulation and is in the hands of “the Council and European Parliament who will have 3 months to exercise their
EC publishes draft regulation on electronic IFUs of Medical Devices
24 June 2011 – From Eucomed e-newsletter – European Commission publishes draft regulation on electronic instructions for use (IFU) of medical devices. ‘Stakeholders can send their comments by 8 August 2011. The Eucomed Alternative Labeling Task Force will meet on 1 July
EU Collective Redress Consultation Paper
Hogan Lovells wrote on 7 FEB ’11 an excellent summary on the situation and status of where the EU is in relation to Collective Redress including a consultation paper that was issued by the EU Commission.
EU RAPEX – System for dangerous consumer goods…
Europa EU Rapid Alert System non-food consumer products (RAPEX): Doesn’t include medical devices, pharmaceuticals, and food http://ht.ly/2twrt Source Europa Webpage http://ht.ly/2twrt for the following information on RAPEX: RAPEX is the EU rapid alert system for dangerous consumer products – with the