BlueReg Team will be pleased to meet you at DIA Europe 2019 in Vienna

28 January 2019


Nadia BOEHRINGER, Anne-Valérie FAUCHER and Caroline Robo (Fesquet) are pleased to invite you to discuss your regulatory and pharmaceutical needs during the DIA Europe 2019 conference in Vienna. Visit our booth located at B48 or contact us in advance to…

eCTD Format Mandatory for EU National Procedures

23 January 2019


After CP, DCP/MRP Procedures, and according to the eSubmissions Roadmap Timelines, eCTD format is now mandatory for all National Procedures in Europe CP Procedure -> eCTD Mandatory from 2010 DCP / MRP Procedures– all regulatory activities -> eCTD mandatory from…

Season’s Greetings & Happy New Year 2019 !

7 January 2019


Best wishes for a Wonderful Christmas Eve, Holidays and a Happy New Year! 🎅 From all BlueReg Team 🎅

Conversion of centrally authorized products into national UK Marketing authorisations in case of No Deal Brexit

4 December 2018


MHRA has sent to Marketing Authorization Holder (MAH) a guidance outlining requirements for submitting baseline information on your product in case of Brexit No Deal Scenario . As MAH, you should be prepared, and BlueReg can provide regulatory and publishing…

Discover our last white Paper

Learn more