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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.
At 4G, our mission is to move the needle in clinical trials. Our robust, efficient approach to RTSM (Randomization and Trial Supply Management) provides enhanced visibility into your trials, enabling you to do your job better and spend your time and resources wisely to get drugs to patients, faster.
RANDOMIZATION
Our team has extensive experience developing complex randomization schemes, including dynamic allocation (adaptive randomization).
Prancer supports central randomization, site blocked randomization, multiple strata, dynamically blocked to strata, dynamically blocked to strata and site as well as multiple randomizations.
Within the past few years, the conversation has shifted from deciding between paper or electronic TMF solutions to instead solidifying what features are required to make an eTMF solution the most optimal. Technology is evolving—and while the life sciences industry has a reputation for being slow to adopt tech advancements in clinical research, it’s catching on to innovations in eTMF pretty quickly.
Buy side or sell side, the Intralinks Dealspace® team is on your side – every step of the way, helping you find the right opportunities, speed due diligence, and close deals faster.
Clinical trials mobile application for us in early phase and Phase I research.
mSource is Medrio's mobile eSource application that includes mPRO, mCapture, and mConsent. All products are native applications and are designed for use in early phase and Phase I research.
mEDU is CFR Part 11 compliant software with CloudEDC™ that is FREE for investigator initiated trials.
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