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Pharmacovigilance activities during clinical trials include: Monitoring adverse events Reporting serious adverse events (SAEs) Signal detection and safety evaluation Risk assessment and mitigation Regulatory safety reporting Together, these activities help ensure that investigational medicinal products are evaluated safely and responsibly

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Gibson, J.B

Reconstituted peptide solutions that are contaminated with bacteria can cause skin infections that dramatically worsen eczema

Are They Studied Together

[2] Gupta V, Awasthi N, Wagner BJ