Falsification protection addresses everyone

You already concluded a contract with EMVO (European Medicines Verification Organisation) for the connection to the European hub? Then you have done the first step to a successful implementation of the requirements of the Delegated Regulation No. 2016/161 (EU). Since your pack data (in particular the serial numbers) will be stored in the national medicines verification systems, you need additional contracts with the respective NMVO (National Medicines Verification Organisation).

Here ACS PharmaProtect GmbH comes into play. As operator of the pharmaceutical industry’s database system in Germany, we are a part of securPharm e.V., the responsible organization for the set-up of a system for the authentication of medicines according the specifications of the Falsified Medicines Directive 2011/62/EU and the Delegated Regulation No. 2016/161 (EU) in Germany.

Already today you can upload your data directly or via the European hub in this database system of the pharmaceutical industry in Germany, make them available for the verification in the pharmacy and test your in-house processes – currently a unique opportunity in Europe.

You just have 603 days left to implement the requirements of the Delegated Regulation in your company. As of the February 9, 2019 medicines without applied safety features cannot be placed on the market.

Conclude the contract with the ACS PharmaProtect GmbH before June 30, 2017 and benefit from the less expensive set-up fee, currently amounting to 20,000 €.

For more information about the contract and the national database system of ACS PharmaProtect please visit our website (www.pharmaprotect.de/en/) and do not hesitate to contact us at:

Phone: +49 30 577 037 900

E-mail: info@pharmaprotect.de

We look forward to welcome you as a participant in the securPharm project.

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