Electronic Informed Consent (eConsent) is the next big technological innovation in clinical trials. 146 respondents from 100 biotech, pharmaceutical, CRO, and IRB organizations shared their experiences, expectations, and ideas about the future of eConsent. Whether you’re just starting to consider eConsent or ready to expand adoption, download this report for insight on what is likely to be the next “must-have” in clinical trials.
For more than 20 years, Bellwyck has been a true partner in developing smarter solutions for the pharmaceutical industry — from clinical trial to commercialization. We utilize cost-efficient packaging strategies to launch clinical studies on time, every time. Discover all of the ways in which Bellwyck might assist you in meeting your unique objectives.
Download the at a Glance Schedule for DIA 2019 Global Annual Meeting - San Diego - June 23-27.
Best-in-class processes coupled with industry-leading technology to fight for your trial’s success.
With unrivaled experience in packaging and labeling, PCI combines knowledge, experience, and innovative technologies ensuring our ability to supply high quality products reliably and effectively wherever in the world our clients need them.
At Syneos Health, we know that negotiation of a site contract is a relatively simple process, which often has an incredibly high number of unintentional complications. Read why many sponsors have entrusted Syneos Health to build a dedicated team with customized tools and processes to provide functional site contracts management services in alignment with their unique R&D strategies and needs. We can help to streamline negotiations and ensure that contract and budget executions are no longer the rate limiting factor in how quickly patient enrollment can begin.
Cytel data scientists apply advanced statistical techniques including predictive modeling of biological processes and drug interactions to unlock the potential of big data. Our team supports biomarker discovery and diagnostic test development based on biomedical signals and images, and real world evidence analysis.
East® version 6.5 continues Cytel’s 20+ years tradition of reliable innovation in the design, monitoring and simulation of clinical trials.
The knowledge we’ve gained from handling millions of international clinical supply shipments has helped us to develop an expertly managed service.
Cytel’s dedicated team of professionals is here to help you address an array of challenges when conducting drug development. Whether you face a complex statistical issue or the need for knowledgeable collaborators to handle biometrics and trial implementation, Cytel has skilled professionals available when you need them.
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