Revue de presse N° 17
Chers adhérents de DMB,
Veuillez trouver ci-dessous la revue de presse n° 17, parution du 31 décembre 2015.
Pour rappel : si vous n’êtes pas inscrits sur un des magazines du site www.samedanltd.com, vous pouvez quand-même accéder au moins à la première partie des articles qui donne déjà une bonne idée du contenu. Par contre seuls les abstracts des articles du DIA Journal ‘Therapeutic Innovation & Regulatory Science’ sont accessibles gratuitement.
Nous tenons aussi à vous rappeler que vous êtes invités à participer à la constitution de cette revue en envoyant tout article que vous souhaiteriez partager avec vos co-adhérents à l’adresse mail suivant: virginie.droal@aixial.com .
DMB vous souhaite une bonne lecture !
Pour l’équipe des contributeurs
Cécile Coustan
Q&A: Investigator Site Data
European Pharmaceutical Contractors, Winter 2015
Through collaborative efforts such as the Shared Investigator Platform, biopharma partners are working to lessen administrative burdens for investigators and enhance the patient experience. Jackie Kent of Eli Lilly and TransCelerate talks to EPC.
http://www.samedanltd.com/magazine/11/issue/244/article/4241
Quality Review (RBM)
International Clinical Trials, Autumn 2015
María Proupín-Pérez of PPH plus says that accurate early identification of main study risks is fundamental when choosing the most appropriate monitoring strategy – contributing to patient safety and quality control, while helping avoid hasty and unwelcome rescue measures.
http://www.samedanltd.com/magazine/13/issue/243/article/4225
Protocol Compliance – Easier with ePRO
International Clinical Trials, Autumn 2015
Exco InTouch’s Laurence Burke examines how sponsors can use mobile ePRO technology to offset protocol complexity and tip the balance in favour of compliance – making life easier for trial participants and investigators, as well as helping ensure greater confidence in data quality.
http://www.samedanltd.com/magazine/13/issue/243/article/4239
New Look at the Arsenal of Technology Solutions
Applied Clinical Trials, October/November 2015
Despite expansion of eClinical solutions, proliferation of vendors and solutions (mature or nascent), companies continues to experience long cycle time drug development. Discover the top 5 technology solutions implemented, those which are less used and the reasons that might explain such a situation!
http://www.appliedclinicaltrialsonline.com/new-look-arsenal-tech-solutions
A Model Data Management Plan Standard Operating Procedure: Results From the DIA Clinical Data Management Community, Committee on Clinical Data Management Plan
Drug information journal, December 2015
A comprehensive template for those who plan to implement or update their Data Management Plan
http://dij.sagepub.com/content/49/5/720.full.pdf+html
WHITE PAPER
Communication related to the use of ePRO in a clinical trial.
https://aws-mdsol-corporate-website-prod.s3.amazonaws.com/Patient-Cloud_Danone-Captures-Quality_20151105_Medidata_Whitepaper_English.pdf.pdf
NEWS
Practical application of CDISC SHARE :
http://www.cdisc.org/cdisc-and-c-path-recently-awarded-fda-grants
The site UnlockCures.org is online since 10 Novembre: Official link