RAPS Euro Convergence 2020 : We are pleased to announce you that Camille Piriou Senior Regulatory Affairs consultant at BlueReg will present "How to successfully launch your product in different markets": From product information to promotional materials. When dealing…
BlueReg Team will attend the Dia Europe in Brussels, from March 17 to 19. Our experts would be there to discuss about your needs concerning Pharmaceutical Development, Regulatory Support, Project Management, CMC, Publishing, Scientific Writing... BlueReg, Nothing But Blue Skies.…
BlueReg Team will attend the CPHI Worldwide in Frankfurt, from November 5 to 7. Our experts would be there to discuss about your needs concerning Pharmaceutical Development, Regulatory Support, Project Management, CDMO Management and Scientific Writing. BlueReg, your partner for…
BlueReg team will attend the TOPRA Symposium in Dublin, from September 30th to October 2nd. Engage with our experts to learn more about our key service offerings covering drug development consulting, drug registration, post authorization, publishing, and medical device regulatory…
BlueReg team will attend the RAPS Regulatory Convergence in Philadelphia, from September 21st to 24th. Engage with our experts to learn more about our key service offerings covering drug development consulting, drug registration, post authorization, publishing and medical device regulatory…
E-regulatory Summit starts in few days! Marlene Schuppli Nollet and Franck VIGLIECCA will be pleased to invite you to discuss your regulatory and publishing needs during the conference in Barcelona. Visit booth 5 or contact us in advance to arrange a…
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 arrange a meeting. Engage with our…
