ClinCard's Tax Toolkit supports research sites and sponsors in remaining IRS Tax compliant while maintaining confidentiality and privacy.
Up to 60% of clinical development time and 40% of cost are spent on patient recruitment. Data can help, but simply accessing more data only muddies your decision making. With Covance, you get the right analysis on the right data to empower your studies. Recruit eligible patients that fit your protocol faster, identify and secure proven and/or new sites, forecast and measure progress more efficiently. With Covance’s proprietary data, your program hits its mark.
New-generation IRT systems go beyond the fundamentals of randomization and drug supply to offer more functionality, visibility, flexibility and quality. Today’s advanced systems allow sponsors to fully control materials management, site and patient interactions, dosing scenarios, and treatment schedules down to individual patient and material unit levels. The IRT Worst Case Scenario Survival Handbook was built from YPrime’s knowledge gained, lessons learned, and creative solutions used to overcome study challenges and keep projects on track, no matter what.
YPrime’s IRT+ goes beyond traditional IRT capabilities of patient randomization and drug supply management with control and a real-time view into critical functions and flows of a clinical trial - involving patient interactions, site activities and clinical supply management.
In this document Yprime shares their knowledge gained, lessons learned, and creative solutions used in overcoming unexpected disruptions in past work to keep projects on track.
YPrime’s eCOA platform offers a combination of quality, speed and flexibility with the ability to support the unique needs of sponsors, sites and patient users. Design and functionality that drives better data quality, efficiency gains, faster decisions, less administrative burden, more project control and great user experiences – add up for big impact.
Cytel’s ACES system supports adaptive design implementation in a secure, audit-trailed environment. ACES facilitates sponsor-committee communications and interim data handling as prescribed by regulatory guidance and according to the study protocol and committee charter.
Clarity is designed for drug and medical device clinical researchers utilizing the latest in Artificial Intelligence to ensure medical records are securely obtained, authenticated and delivered to requestors with the most efficient process possible. Developed in collaboration with Health Information Management, Clarity ensures that the release of protected health information is preformed accurately, securely and with an understanding that each record represents a real person.
Vault is designed for life sciences organizations that require ubiquitous access to clinical data. Vault leverages the Artificial Intelligence tools across the HealthSource platform as well as a HiTrust data storage environment to create a unified member-centric data repository. Vault creates a unified patient and provider centric data repository. Together with Smart Chart, these products drive more powerful clinical outcome-based models.
Smart Chart is designed for life sciences companies that require clinical data for improved decision making. Smart Chart quickly identifies and extracts heath data from structured and unstructured medical records and supplemental data feeds to aggregate a patient’s medical history into a longitudinal digital profile.
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