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…

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…

Corinne Schmitz, experte de l’industrie pharmaceutique

30 August 2018


This week, “La Tribune” and its partner Bpifrance have decided to present Corinne Schmitz, CEO of BlueReg Group as a woman entrepreneur. BlueReg is constantly evolving, and regroup now 60 full time highly qualified, and has worked with 100 clients…

Discover our last white Paper

Learn more