Q&A Ongoing

Q&A on Good Clinical Practice (GCP)

EMA · 2024 European Medicines Agency

ABSTRACT — EDITORS' SUMMARY

Continuously updated GCP Q&A from the GCP IWG. Practical inspector expectations on CRFs, eligibility verification, computerised systems, source data definition, and essential documents.

LIVE SOURCE · CONTINUOUSLY UPDATED

Read live on www.ema.europa.eu ↗

METADATA

TypeQ&A

Year2024

VersionOngoing

StatusCurrent

FormatHTML

Pages—

Size—

Last reviewedJAN 2024

SOURCE

HTML · CANONICAL LINK https://www.ema.europa.eu/en/human-regulatory-overview/research-development/compliance-research-development/good-clinical-practice/qa-good-clinical-practice-gcp ↗

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