Human medicines European public assessment report (EPAR): Rixubis, nonacog gamma, Date of authorisation: 19/12/2014, Revision: 12, Status: Authorised

Human medicines European public assessment report (EPAR): Rixubis, nonacog gamma, Date of authorisation: 19/12/2014, Revision: 12, Status: Authorised

Human medicines European public assessment report (EPAR): Vaniqa, eflornithine, Date of authorisation: 19/03/2001, Revision: 24, Status: Authorised

Human medicines European public assessment report (EPAR): Vaniqa, eflornithine, Date of authorisation: 19/03/2001, Revision: 24, Status: Authorised

Human medicines European public assessment report (EPAR): Cervarix, human papillomavirus vaccine [types 16, 18] (recombinant, adjuvanted, adsorbed), Date of authorisation: 20/09/2007, Revision: 42, Status: Authorised

Human medicines European public assessment report (EPAR): Cervarix, human papillomavirus vaccine [types 16, 18] (recombinant, adjuvanted, adsorbed), Date of authorisation: 20/09/2007, Revision: 42, Status: Authorised

LinkedIn Live session: Improving efficiency of approval process for new medicines in the EU , Online, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 5 December 2024, 12:30 (CET) to 5 December 2024, 13:30 (CET)

LinkedIn Live session: Improving efficiency of approval process for new medicines in the EU , Online, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 5 December 2024, 12:30 (CET) to 5 December 2024, 13:30 (CET)

Newsletters

Stay informed on our latest news!

CAPTCHA

This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.

randomness