Patient Engagement Suite
Protocol Amendments And Electronic Consent: Overcoming The Challenges To Reap The Benefits
Learn about some insights that have been gleaned from experience deploying eConsent on diverse trial types around the world.
IRT And Direct-To-Patient Trials
Want to know more about the growth and expansion for IRT in the decentralized trial space? Witness how IRT is being used to support direct-to-patient delivery in this hybrid trial case study presentation.
Climbing The Ladder To Higher Electronic Consent Adoption
When it comes to gaining the benefits of eConsent in clinical trials, site adoption is the key. Explore the steps up the ladder of eConsent adoption to reach new heights with every study.
Intelligent IRT Design Process For COVID-19 Trials Accelerates Digital Enablement At Sites
Cenduit IRT study design teams took on the challenges pressing biopharmaceutical industry sponsors as they worked to digitally enable sites and speed up time to first-patient-in for COVID-19 therapeutic and vaccine trials.
IRT And eClinical Technology Considerations For Cell And Gene Therapy
Don't try to fit cell and gene therapy studies – or any kind of study – into pre-defined functionality. The Cenduit IRT and Quantum Interactive™ agile design platforms and reporting tools support clients’ most complex requirements.
Navigating The Use Of Controlled Substances In Clinical Trials Using IRT
Sponsor organizations that want to use controlled substances in clinical studies must manage the associated regulatory and logistical requirements. Read how this can be challenging for emerging biopharma.
Successful Solutions For Drug Accountability & Returns Management
See how sponsors are using electronic solutions for Drug Accountability (DA) and experiencing significant increase in efficiency and accuracy that these methods provide.
Removing The Barriers To eConsent Adoption
eConsent technology has existed for nearly 20 years in various iterations. Read how sponsors have taken a cautious approach to using eConsent, piloting it on individual studies but refraining from incorporating it across all pipelines in clinical operations.
IQVIA Complete Consent
IQVIA Complete Consent combines a friendly, feature-rich technology platform that patients and sites are eager to use, with the powerful, scalable, operational infrastructure that sponsors need to make global implementations successful.
Tips For Overcoming Today's Drug Supply Challenges Through Technology
In this webinar, explore how to manage a supply chain through IRT with self service tools and actionable insights as well as best practices for supply forecasting and overstock management.