Developments, news and strategies for drug development specific to phase I through Phase III global clinical trial management, execution, project management and outsourcing. Go→
News, articles and issues specific to clinical trial practice and implementation at the investigative site level. Go→
Strategies and innovations related to how clinical professionals are utilizing technology internal and external to their organizations to advance clinical trials. Go→
News, articles and issues specific to laboratories role in the clinical trial, including ECG, imaging, genotyping, tissue samples and more. Go→
News, developments and strategies for clinical trials conduct in relation to the FDA, EMEA and other global regulatory authorities overseeing the drug development industry. Go→
News, articles and strategies related to clinical trial design which impact postmarketing studies, therapeutic areas, adaptive trials, statistics, protocols and more. Go→
PharmaStart, a CRO with offices in Illinois, Ohio, North Carolina, California and London, has implemented Veeva System's Valut eTMF solution.
Users of PharmaStart's new solution include its internal teams, clinical partners, and its 75+ investigator sites around the globe. The CRO chose a cloud-based solution for real-time access, improved productivity, as well as a reduction in paper. The Vault eTMF allows PharmStart's processes and workflows to be automated so individual sites pull down a template, complete it, and upload it back into Vault for stakeholder visibility in real time. In addition, placement into the eTMF happens automatically. The company maintains it has addressed hidden cost savings as TMF documents are uploaded, QC’d, and approved in the system along the way. For study start-up, there is less need for managing documents and signatures, and at study close-out eliminates the document reconciliation process.
Read the full release here.