According to Michele Russell-Einhorn, Chief Compliance Officer at Advarra, most research institutions had taken steps to partially or fully suspend…
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According to Michele Russell-Einhorn, Chief Compliance Officer at Advarra, most research institutions had taken steps to partially or fully suspend…
- Daenya McDonald, Marketing Director at Clinical Research IO 1 week agoExplore CRIO’s integrated eSource/electronic medical record (EMR)/electronic data capture (EDC) model, where source data is collected electronically by the site…
- Team CRIO 1 week agoHere’s something new we know you’ll love. Do more with better data when your site enables CRIO’s Recruiting API. Now…
- Daenya McDonald, Marketing Director at CRIO 4 months agoMark Joing is the Founder & CEO at Mojo Trials, a startup life sciences service provider delivering virtual site monitoring…
- Mark Joing, Founder & CEO at Mojo Trials 5 months agoBridging the gap eSource is the bridge between the protocol and the eCRF fields. To understand why, we need to…
- Raymond Nomizu, CEO & Co-Founder at Clinical Research IO (CRIO) 5 months ago73% of sites reported using paper as the primary means of data collection In a 2018 CRIO site survey with…
- Raymond Nomizu, CEO & Co-Founder at Clinical Research IO (CRIO) 6 months agoCRIO Publisher is one of CRIO’s most highly anticipated new releases. It’s all part of our vision to remove redundancies…
- Daenya McDonald, Marketing Director at Clinical Research IO 6 months agoHire your dream Clinical Research Coordinator. Reveal your applicant’s true capabilities with these 10 questions. When I interviewed for my…
- Anna Krauss, Customer Success at Clinical Research IO 4 years agoAchieving representative enrollment – meaning diversity in race, age, gender and socioeconomic status – in clinical trials is essential to…
- Maxine Lai, Content Associate at Clinical Research IO 2 years agoDisclaimer: The examples noted in the following article are all firsthand accounts of the author, but for the purpose of…
- Takoda Roland, CCRA, CCRP, CNA, Founder of Philadelphia Pharmaceutical Research 2 years agoMost discussion about electronic source (eSource) documentation in the clinical research enterprise starts from a sponsor standpoint, with eSource being…
- Raymond Nomizu, CEO of Clinical Research IO 5 years agoHear what it feels like to endure an FDA audit as a Principal Investigator or clinical research site owner, based…
- Bob Bedetti, Business Development at Clinical Research IO 2 years agoElectronic Source (eSource) and Electronic Data Capture (EDC) are increasingly popular technologies for collecting and managing clinical trial data. The…
- Phoebe Stoye, Product Manager at Clinical Research IO 2 years agoYour study doesn't stop just because you're out of town or not in a clinic.
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