Decision of the Executive Director on transparency measures for senior staff leaving the Agency
Decision of the Executive Director on transparency measures for senior staff leaving the Agency
Decision of the Executive Director on transparency measures for senior staff leaving the Agency
Joint Committee Opinion 27/2020 on criteria and restrictions for senior staff applying for occupational activities within two years after leaving the Agency
Establishing efficacy based on single-arm trials submitted as pivotal evidence in a marketing authorisation
Reflection paper on establishing efficacy based on single-arm trials submitted as pivotal evidence in a marketing authorisation application
Guidance for competent authorities on how to highlight VNRAs
Agenda of the CHMP meeting 16-19 September 2024
Human medicines European public assessment report (EPAR): Bonviva, ibandronic acid, Date of authorisation: 23/02/2004, Revision: 31, Status: Authorised
Human medicines European public assessment report (EPAR): Bondronat, ibandronic acid, Date of authorisation: 25/06/1996, Revision: 34, Status: Authorised
IRIS guide for applicants - How to create and submit scientific applications, for industry and individual applicants
Early dialogue with healthcare professional organisations for marketing authorisation applications: 1-year report