news roundup
INC Research expanded its functional provider services (FSP) offerings by adding investigator payment processing.
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Manual errors jeopardizing your data quality and regulatory review process? Get expert data-saving solutions on the industry's first educational and training portal, designed exclusively for the Clinical Development Professional.
CTA: Explore Almac Clinical University
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ICON annnouned that the FDA has awarded the company with a project validating three Patient Reported Outcomes instruments that will measure clinical endpoints in antibacterial drug trials. |
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Help our industry better understand the drivers, benefits, and barriers of a unified clinical operating model. Survey participants will be the first to receive the report when we release it later this year.
Take the
 Veeva 2017 Unified Clinical Operations Survey
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The collaboration gives PPD access to Frenova's global nephrology experts, as well as Frenova's exclusive alliance of research sites, which encompass 260 research sites with 450 principal investigators and access to more than 183,000 active ESRD patients and 390,000 active CKD patients.
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Are Local IRBs Really Necessary?
Live Webinar: Tuesday, February 28 at 1:00pm EST
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Articles
Learn from our expert technology panel how various trends and technologies interrelate to comprise the clinical trial of tomorrow.
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To better examine the different use cases and needs of clinical trial technology, it is important to consider each unique user group or role, including clinical site pharmacists and clinical research nurses. |
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Blog Posts
A recent EU symposium on rare diseases called for collaboration and avowals of readiness to work together, along with repeated insistence on the urgency of finding solutions, on the need for bureaucrats to move fast, and on greater attention to patient thinking.
All stakeholders – sites, inspectors, sponsors, CROs, and vendors - are welcome to take the non-commercial TMF Reference Model's state-of-the-industry 2017 TMF Survey, designed to provide insights for both paper and electronic trial document management. |
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RBM
TransCelerate's recently released RBM interactive guide is to provide the broader community of stakeholders--including other sponsors that are not members of TransCelerate-- to help facilitate the adoption and implementation of RBM.
The ICH GCP E6 R2 puts more onus on sponsors, investigators, and CROs and requires sponsors to adopt adequate processes for monitoring trial activity, communicating across sites, and maintaining data integrity.
This checklist offers sponsors' insight into the questions and the type of answers CROs should provide. |
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