Uncover how Flatiron Clinical Pipe™ significantly reduced inefficiencies and errors in cancer clinical trials by automating data transfer, cutting CRF submission time to just 43 seconds.
Here, we explore an end-to-end clinical data science platform designed to streamline the rapid generation of deep insights from clinical trial data, enabling the efficient delivery of crucial analyses.
Learn how to automate the flow of serious adverse event (SAE) information between data management and safety systems, enabling more timely responses by Pharmacovigilance (PV) teams.
Gather data directly from the patient — the true source. Empower your team to streamline data collection, making it faster and easier for everyone involved.
A responsive solution, unearth how IQVIA's electronic clinical outcome assessments are leveraging technology to gather valuable insights about the patient and caregiver experience.
In this two-minute video, viewers will learn how Veeva Clinical Database (CDB) aggregates, cleans, and transforms clinical data from various sources, including third-party EDCs.
Having the right tools to build intuitive and patient-friendly eCOA solutions can simplify trial complexity, reduce participation burden, and drive engagement and compliance.
Compare different types of wearable devices to find the optimal solution for your study, and consider how integration can elevate your clinical development program to new heights.
Discover how Medable's platform technology enabled a top vaccine developer to accelerate study deployment and recruitment timelines by watching this live demo.
With so much at stake, consider partnering with an expert in clinical outcome assessments and decentralized clinical trials. Learn what sets us apart from others in the industry.
Start enabling easier tracking, management, and oversight of consent status, eICF distribution, IRB approval status, site staff signatures, monitoring workflows, and other operational tasks.
