Regulatory document
Committee for Medicinal Products for Human Use (CHMP) Biologics Working Party (BWP)…
EMA · Guidance · EU
Key facts
| Title | Committee for Medicinal Products for Human Use (CHMP) Biologics Working Party (BWP) stakeholders' meeting on the Guideline on the requirements for quality documentation concerning biological investigational medicinal products (IMP) in clinical trials |
|---|---|
| Issuer | European Medicines Agency |
| Source | EMA |
| Document type | Guidance |
| Country or region | EU |
| Document | ema.europa.eu |
| Issuer website | ema.europa.eu |
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