CPMP

E130560

CPMP is the former scientific committee of the European Medicines Agency responsible for evaluating and providing opinions on the quality, safety, and efficacy of human medicinal products in the EU.

All labels observed (1)

Label Occurrences
CPMP canonical 2

How this entity was disambiguated

Statements (41)

Predicate Object
instanceOf European Union body
regulatory committee
scientific committee
abbreviationOf Committee for Proprietary Medicinal Products
acronym CPMP self-link
activity adoption of scientific guidelines for human medicines
coordination of benefit-risk assessment of medicines
provision of expert advice to the European Commission
country European Union
domain human medicinal products
field drug evaluation
pharmaceutical regulation
public health
fullName Committee for Proprietary Medicinal Products
goal ensuring that human medicines in the EU are safe, effective and of high quality
protection of public health in the European Union
jurisdiction European Union
language English
locatedIn London, England
surface form: London

United Kingdom
parentOrganization European Medicines Agency
partOf EMA
Committee for Medicinal Products for Human Use
surface form: European Medicines Agency
regulatoryFramework European Union pharmaceutical legislation
regulatoryRole advising on EU-wide marketing authorisations
harmonisation of medicinal product evaluation in the EU
providing scientific opinions on marketing authorisation applications
replacedBy Committee for Medicinal Products for Human Use
surface form: CHMP

Committee for Medicinal Products for Human Use
reportsTo European Commission
responsibleFor assessment of efficacy of human medicines
assessment of quality of human medicines
assessment of safety of human medicines
evaluation of human medicinal products
scope proprietary medicinal products
sector human medicines
status former committee
successor Committee for Medicinal Products for Human Use
surface form: CHMP

Committee for Medicinal Products for Human Use
typeOfOrganization scientific advisory committee
worksWith national competent authorities of EU Member States

How these facts were elicited

Referenced by (2)

Full triples — surface form annotated when it differs from this entity's canonical label.