Clinical Trial Information System (CTIS) structured data form - Initial application, additional Member State Concerned, substantial modification, non-substantial modification

Clinical Trial Information System (CTIS) structured data form - Initial application, additional Member State Concerned, substantial modification, non-substantial modification

Human medicines European public assessment report (EPAR): Zydelig, idelalisib, Date of authorisation: 18/09/2014, Revision: 21, Status: Authorised

Human medicines European public assessment report (EPAR): Zydelig, idelalisib, Date of authorisation: 18/09/2014, Revision: 21, Status: Authorised

Human medicines European public assessment report (EPAR): Amyvid, florbetapir (18F), Date of authorisation: 14/01/2013, Revision: 15, Status: Authorised

Human medicines European public assessment report (EPAR): Amyvid, florbetapir (18F), Date of authorisation: 14/01/2013, Revision: 15, Status: Authorised

Veterinary medicines European public assessment report (EPAR): Purevax RC, vaccine against feline viral rhinotracheitis and feline calicivirosis, Status: Authorised

Veterinary medicines European public assessment report (EPAR): Purevax RC, vaccine against feline viral rhinotracheitis and feline calicivirosis, Status: Authorised

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