EC directive to protect against counterfeit medicines
EU Directive 2011/62/EU prescribes how the accountability of manufacturers and batches as well as anti-tampering protection must be guaranteed in the future. The implementation of the EU Directive is planned for 2016 at the latest. It is planned for the new safety standard to be implemented using a 2D DataMatrix code, which will be printed onto the packaging. The anti-counterfeit system has been described in detail by securPharm
We are already well-prepared for this.