Commission Recommendation 2013/172/UE, of 5 of April 2013
Recommendation regarding a unified system of identification of medical devices within the Union.
Production of Medicinal Products Human Consumption
Commission Implementing Decision 2013/196/UE, of 24 of April 2013
Amends the Execution Decision 2012/715/EU, which establishes a list of third countries with regulation applicable to substances destined for the production of medicinal products human consumption and corresponding measures of control and execution that ensures a level of health protection equivalent to the one in place in the European Union.