Certificates of Suitability (CEP)

E82718

Certificates of Suitability (CEP) are official documents that certify a substance’s compliance with European Pharmacopoeia standards, streamlining its use in pharmaceutical products across Europe.

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AI-generated illustration of Certificates of Suitability (CEP)

This AI-generated illustration was produced by black-forest-labs/FLUX.2-dev (1024x1024) from a prompt written by openai/gpt-oss-120b from the entity's label + description.

Prompt

Generate an image of a certificates of Suitability (CEP) (Certificates of Suitability (CEP) are official documents that certify a substance’s compliance with European Pharmacopoeia standards, streamlining its use in pharmaceutical products across Europe.)

All labels observed (1)

Label Occurrences
Certificates of Suitability (CEP) canonical 1

How this entity was disambiguated

Statements (48)

Predicate Object
instanceOf European Pharmacopoeia certificate ⓘ
pharmaceutical regulatory document ⓘ
abbreviation CEP ⓘ
applicationSubmittedBy manufacturer of the substance ⓘ
applicationSubmittedTo EDQM ⓘ
appliesTo active pharmaceutical ingredients ⓘ
excipients used in medicinal products ⓘ
substances used in pharmaceutical manufacturing ⓘ
basedOn European Pharmacopoeia monographs ⓘ
benefit facilitates mutual recognition of substance quality across Europe ⓘ
protects confidential manufacturing information of the substance manufacturer ⓘ
reduces regulatory workload for national authorities ⓘ
containsInformationOn compliance with specific European Pharmacopoeia monographs ⓘ
impurity profile of the substance ⓘ
manufacturing process of the substance ⓘ
quality control of the substance ⓘ
evaluationIncludes assessment of analytical methods ⓘ
assessment of impurity controls ⓘ
assessment of manufacturing documentation ⓘ
format unique certificate number identifying the substance and holder ⓘ
fullName Certificates of Suitability to the monographs of the European Pharmacopoeia ⓘ
holder company to which the CEP is granted ⓘ
issuedBy EDQM ⓘ
European Directorate for the Quality of Medicines & HealthCare ⓘ
jurisdiction Council of Europe ⓘ
language issued in English or French ⓘ
legalStatus voluntary alternative to full substance documentation in marketing authorisation dossiers ⓘ
purpose avoid duplication of quality assessments by national authorities ⓘ
demonstrate compliance of a substance with European Pharmacopoeia standards ⓘ
simplify marketing authorisation applications for medicinal products ⓘ
streamline use of substances in pharmaceutical products across Europe ⓘ
recognizedBy European Medicines Agency ⓘ
European medicines regulatory authorities ⓘ
national competent authorities in Europe ⓘ
regulatoryScope quality of active substances ⓘ
quality of certain starting materials ⓘ
quality of excipients ⓘ
relatedTo European Pharmacopoeia ⓘ
active substance master file system ⓘ
subjectTo inspections of manufacturing sites ⓘ
post-certification surveillance by EDQM ⓘ
revision or withdrawal in case of non-compliance ⓘ
usedBy API manufacturers ⓘ
pharmaceutical companies ⓘ
regulatory authorities ⓘ
usedIn marketing authorisation applications for medicinal products ⓘ
variation applications for medicinal products ⓘ
validity time-limited and subject to renewal ⓘ

How these facts were elicited

Referenced by (1)

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