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Implementing a centralised pharmacovigilance service in a non-commercial setting in the United Kingdom
The implementation of a pharmacovigilance service compliant with the legal and regulatory responsibilities of clinical trial sponsors presents particular challenges for sponsors in a non-commercial setting. In this paper we examine these challenges in detail. We identify and discuss the key steps in...
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| Hoofdauteurs: | , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2013
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3695787/ https://ncbi.nlm.nih.gov/pubmed/23758677 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1745-6215-14-171 |
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