Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/07/30 23:20:53」(JST)
wiki en
English Journal
- Assessing the detection, reporting and investigation of adverse events in clinical trial protocols implemented in Cameroon: a documentary review of clinical trial protocols.
- Ebile AW1,2, Ateudjieu J3,4,5, Yakum MN6,7, Djuidje MN8,9, Watcho P10.
- BMC medical ethics.BMC Med Ethics.2015 Sep 29;16(1):67. doi: 10.1186/s12910-015-0061-5.
- BACKGROUND: International guidelines recommend ethical and scientific quality standards for managing and reporting adverse events occurring during clinical trials to competent research ethics committees and regulatory authorities. The purpose of this study was to determine whether clinical trial pro
- PMID 26420169
- Lessons learnt from enrolment and follow up of pregnant women and their infants in clinical trials in South Africa, a low-middle income country.
- Cutland CL1, Cunnington M2, Olugbosi M3, Jones SA4, Hugo A4, Maharaj K4, Slobod K3, Madhi SA5.
- Vaccine.Vaccine.2015 Sep 24. pii: S0264-410X(15)01167-6. doi: 10.1016/j.vaccine.2015.08.040. [Epub ahead of print]
- INTRODUCTION: Infectious causes are a significant contributor to morbidity and mortality in neonates and young infants. Immunization of pregnant women to protect the mother and/or her infant is gaining momentum due to the benefits of this strategy demonstrated in numerous implemented strategies (Mat
- PMID 26409812
- Data monitoring committees for pragmatic clinical trials.
- Ellenberg SS1, Culbertson R2, Gillen DL3, Goodman S4, Schrandt S5, Zirkle M5.
- Clinical trials (London, England).Clin Trials.2015 Sep 15. pii: 1740774515597697. [Epub ahead of print]
- In any clinical trial, it is essential to monitor the accumulating data to be sure that the trial continues to be safe for participants and that the trial is being conducted properly. Data monitoring committees, independent expert panels who undertake regular reviews of the data as the trial progres
- PMID 26374679
Related Links
- National Institutes of Health (NIH) National Institute of Dental and Craniofacial Research (NIDCR) I. Roles and Responsibilities The Data and Safety Monitoring Board (DSMB) is an independent group of experts that ...
- DSMB Data & Safety Monitoring Board Clinical research A committee of independent clinical research experts who review data in ongoing clinical trials, ensuring that participants are not exposed to undue risk, and look for any ...
Related Pictures
★リンクテーブル★
| リンク元 | 「データ安全性モニタリング委員」 |
| 関連記事 | 「DSM」「DS」 |
「データ安全性モニタリング委員」
- 英
- Data and Safety Monitoring Board DSMB
- 関
- 独立データモニタリング委員会/効果安全性評価委員会 Independent Data Monitoring Committee (IDMC)
- データ及び安全性モニタリング委員会 モニタリング委員会 Monitoring Committee データモニタリング委員会 Data Monitoring Committee
- 臨床試験の進行状況、安全性データ及び重要な有効性評価項目を何回かにわたって評価するとともに、治験依頼者に試験の継続、修正、又は中止を勧告するために、治験依頼者が必要に応じて設立する委員会。