Overview of clinical trials vigilance units in French institutional sponsors – A study from the REVISE working group-Reference-Cited by-同舟云学术

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Overview of clinical trials vigilance units in French institutional sponsors – A study from the REVISE working group

Published:2021-11 Issue:6 Volume:76 Page:743-750
ISSN:0040-5957
Container-title:Therapies
language:en
Short-container-title:Therapies

Author:

Petitpain Nadine,Olivier Pascale,Crépin Sabrina^ORCID,Leone Emanuela,Ouk Thavarak,Villeneuve Claire^ORCID,Muller Charlotte,Ruault Sophie,Jamet Aurélie^ORCID,Franceschi Marie-Paule,Duranton Sophie^ORCID,Gavard Marylaure^ORCID

Publisher

Elsevier BV

Subject

Pharmacology (medical)

Reference12 articles.

1. The limitations of observation studies for decision making regarding drugs efficacy and safety;Gueyffier;Therapie,2019

2. How the new European data protection regulation affects clinical research and recommendations?;Demotes-Mainard;Therapie,2019

3. Quality of serious adverse events reporting to academic sponsors of clinical trials: far from optimal: quality of SAE reporting to academic sponsors;Crépin;Pharmacoepidemiol Drug Saf,2016

4. The reporting of harms in publications on randomized controlled trials funded by the “Programme hospitalier de recherche clinique,” a French academic funding scheme;Favier;Clin Trials,2018

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Overview of literature monitoring practice of clinical trials vigilance units in French institutional sponsors – A study from the REVISE working group;Therapies;2023-11

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