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ANALYSIS OF INTERNATIONAL REQUIREMENTS FOR DESIGNING OF CLINICAL TRIALS
During the analysis of international requirements for designing of clinical trials we found that principal documents are provided by ICH. The main standard in Russian Federation is the National State Standard “Good Clinical Practice”, that is similar to ICH GCP. Thorough industrial standards are iss...
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| Hlavní autoři: | , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Russo |
| Vydáno: |
LLC Center of Pharmaceutical Analytics (LLC «CPHA»)
2019-01-01
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| Edice: | Разработка и регистрация лекарственных средств |
| Témata: | |
| On-line přístup: | https://www.pharmjournal.ru/jour/article/view/99 |
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