Clinical Trial Information System (CTIS) structured data form - Initial application, additional Member State Concerned, substantial modification, non-substantial modification
Big data training curriculum
Human medicines European public assessment report (EPAR): Zydelig, idelalisib, Date of authorisation: 18/09/2014, Revision: 21, Status: Authorised
Agenda - ACT EU multi-stakeholder platform annual meeting
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Three-year work plan for the Quality Drafting Group (QDG) of the Committee on Herbal Medicinal Products (HMPC)
Veterinary medicines European public assessment report (EPAR): Purevax RC, vaccine against feline viral rhinotracheitis and feline calicivirosis, Status: Authorised
Questions and answers about the clinical study data proof-of-concept pilot for industry
Guideline on quality data requirements for applications for biological veterinary medicinal products intended for limited markets
Quality data requirements for applications for biological veterinary medicinal products intended for limited markets - Scientific guideline