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An Automated Standardized System for Managing Adverse Events in Clinical Research Networks
Multi-site clinical protocols and clinical research networks require tools to manage and monitor adverse events (AEs). To be successful, these tools must be designed to comply with applicable regulatory requirements, reflect current data standards, international directives and advances in pharmacovi...
Guardat en:
| Publicat a: | Drug Saf |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2008
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6602073/ https://ncbi.nlm.nih.gov/pubmed/18759506 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2165/00002018-200831100-00001 |
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