EMVO Announcement to Future On - Boarding
18.04.2018
NGDA : N-Ident Registrierung gestartet
03.04.2018
Die N-Ident Registrierung ist ab dem heutigen Tag über das Portal der NGDA möglich. Damit wird ein weiterer Meilenstein auf dem Weg zur fälschungssicheren Medikamentenabgabe erreicht. Ziel ist es, ab dem 9. Februar 2019 alle verschreibungspflichtigen Arzneimittel vor Abgabe an den Patienten einer Echtheitsprüfung unterziehen zu können. Dies geht aus …
Status Report 2018 available
15.02.2018
One year before the Delegated Regulation applies, securPharm has released it’s new status report.
New FAQ (version 9) of the EU Commission
13.02.2018
The EU Commission has published in february 2018 its new FAQ document (version 9) to the Falsified Medicines Directive 2011/62/EU and the Delegated Regulation (EU) 2016/161.
New FAQ (version 8) of the EU Commission
23.11.2017
The EU Commission has published in November 2017 its new FAQ document (Version 8) to the Falsified Medicines Directive 2011/62/EU and the Delegated Regulation (EU) 2016/161.
New FAQ (version 7) of the EU Commission
21.06.2017
The EU Commission has published in November 2017 its new FAQ document (version 7) to the Falsified Medicines Directive 2011/62/EU and the Delegated Regulation (EU) 2016/161.
Coding Rules 2.03 (incl. multi market packs)
16.05.2017
securPharm has released its new coding rules (v. 2.03). These now include detailed rules for multi market packs for the German market. For convenience there is also a changelog listing all changes to the former Version.
