This post is on the newly published Commission Regulation (EU) No 722/2012 of 8 August 2012 “concerning particular requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC with respect to active implantable medical devices and medical devices manufactured utilising tissues of animal origin” which was published in the Official Journal of the European Union on 9 August 2012.
The post on this Commission Regulation (EU) No 722/2012 is thx to Erik Vollebregt who blogs on EU legal and regulatory developments of medical devices. Erik has provided content previously to our blog and we thank him for his generosity in allowing us to post his content.
Medical Devices Utilizing Tissues of Animal Origin New EU Commission Regulation