Global Academic Research Organization UCL Selects Phlexglobal s Innovative eTMF Solution to Enhance TMF Compliance and Inspection-Readiness Across Entire Study Portfolio prweb.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from prweb.com Daily Mail and Mail on Sunday newspapers.
MIAMI, June 3, 2021 /PRNewswire/ ArisGlobal, the leading provider of software that automates core product development functions for over 300 global life sciences companies, today released
Amersham, UK; Malvern, PA. (PRWEB) June 02, 2021 Phlexglobal, a leading innovative technology and services provider for the life sciences industry, today
05.11.21 Clinical Trial Software And Service Partners Ready To Help
With the exponential number and increasing complexity of clinical studies now being run the paper-based informed consent process is inherently inefficient. Rave eConsent is an innovative, patient-friendly, electronic informed consent and patient enrollment system for clinical trials.
Our industry is now, more than ever, ready to move to decentralized trials (DCT) and design hybrid protocols that support trial continuity and have a more patient-centric approach. Most sponsors have struggled to implement DCT and need an innovative, modern technology platform that enables more efficient and future-ready trial processes. The unique architecture of encapsia brings the technology to the data and provides an agile, revolutionary way to support decentralized clinical trial.
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PLEASANTON, Calif., April 20, 2021 /PRNewswire/ Increasing complexity in medtech clinical trials and changing regulations like EU MDR and IVDR require data collection and analysis on a much larger scale. To better manage data and speed time to market, more fast-growing device and diagnostics companies are adopting Veeva MedTech solutions. Gala Therapeutics, Inari Medical, and Lumicell use Veeva MedTech Vault Clinical Suite applications from Veeva Systems (NYSE: VEEV) to conduct and manage trials while maintaining inspection readiness.
Veeva MedTech solutions bring together content and processes to simplify trial execution and ensure compliance. For medtech, adopting advanced clinical applications is a foundational step to meet unique data requirements and regulations and enable faster product development.