Clinical Technologies Solutions
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Streamline Your Regulatory Process
1/18/2022
The Advarra eRegulatory Management System (Advarra eReg) provides integrated protocol, staff, and institution documentation to streamline regulatory process and enhance compliance.
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Accelerate Study Startup Through Better Collaboration
3/3/2025
With 80% of trials failing to enroll patients on time, improved collaboration between sites and sponsors is essential.
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Flexible Solutions To Facilitate Comprehension And Compliance
9/18/2024
Effective consent goes beyond signatures. Learn how to enhance participant understanding, streamlines document management, and improve workflow efficiency, to reduce errors and inspection risks.
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Medidata Sensors
1/7/2026
For clinicians and study managers, this end-to-end solution offers powerful study management, monitoring, and reporting tools that enable real-time visibility into patient compliance, data quality, and study progress.
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Digital Biomarkers Solution May Enable Smaller, Faster Clinical Trials
7/8/2024
See how sponsors of Huntington’s disease (HD) clinical trials can potentially obtain earlier indications of progress by utilizing digital biomarkers.
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TrialKit eConsent
11/18/2024
Help your patients make informed decisions without burying them in paper
With electronic informed consent (eConsent) software, your patients can access consent forms using any device they choose. And because it’s part of TrialKit’s unified platform, both your patients and your study team get a seamless experience.
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NetSuite For The Biotechnology Industry
11/15/2024
Biotech companies progressing through clinical trials, planning an IPO, and undergoing rapid growth have a unique set of financial, contract, compliance, and reporting needs. We have designed an ERP solution, built on NetSuite, to address all of these needs. With over 50 implementations in the last two years alone, SuiteSuccess for Life Sciences is quickly becoming the defacto software standard for all successful biotechnology companies.
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Medical Writing Software
6/17/2025
Accelerate Medical Writing Without Compromising Accuracy or Compliance
In the fast-paced world of clinical research, the ability to produce, review, and finalize high-quality documents—on time and with full regulatory compliance—is non-negotiable. Ideagen Document Review (formerly known as PleaseReview) is the trusted collaboration and co-authoring platform that enables clinical teams to streamline document reviews, reduce version chaos, and ensure traceable, auditable feedback across the board.
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Revvity Signals Software Risk-Based Monitoring Solution
8/28/2017
The Revvity Signals Software Risk-Based Monitoring Solution is the most effective way to leverage data-driven insights to optimize site performance while improving patient safety.
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Sensors and Wearables: Gain Deeper Insights
6/17/2024
Collect valuable data on treatment effects beyond clinic visits and without burdening patients or sites using mobile health sensors and wearables with secure data collection.