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Main changes in European Clinical Trials Regulation (No 536/2014)
The new Regulation (EU) No. 536/2014 for clinical trials of medicinal products for human is part of a European regulatory framework in which the European Commission has wished to give a strong impetus to scientific research and industrial progress. It is a new regulation that fills a series of regul...
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| I publikationen: | Contemp Clin Trials Commun |
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| Huvudupphovsmän: | , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Elsevier
2018
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6039537/ https://ncbi.nlm.nih.gov/pubmed/30003173 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.conctc.2018.05.014 |
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