Clinical Technologies Solutions

  1. Rave eTMF - Simplify Trial Oversight With Unified Document Management 1/2/2023

    Your Trial Master File (TMF) complexity is growing. It’s not uncommon to upload thousands of documents per day, subject to strict regulatory requirements for filing, and under aggressive timelines. Rave eTMF is a global, secure collaboration platform to seamlessly manage Trial Master File content so it is always contemporaneous with the study.

  2. Unified Platform Solutions For Phase I Clinical Trials 3/19/2024

    Phase I clinical trials need technological solutions that support rapid implementation and end-to-end processes. Signant’s unified eClinical platform provides the perfect partner for Phase I research.

  3. TrialKit Picture Archiving and Communication System (PACS) 12/6/2024

    Whether you’re conducting an oncology trial, a neurology study, or imaging-based endpoint research, TrialKit’s flexible imaging capabilities can meet your needs.

  4. Simulants: Unlock Insights And Accelerate Medical Breakthroughs 11/17/2023

    Get an overview of this groundbreaking synthetic data product – uniquely derived from Medidata’s exclusive repository of global, standardized historical clinical trial data.

  5. Vaccine Trial Solutions 12/9/2024

    Signant streamlines vaccine trials with efficient data collection, enhanced engagement, and simplified operations—ensuring quality, compliance, and faster market entry.

  6. Transforming Medical Data Into Research Insights 10/19/2023

    Discover the efficiency and security of automated, precise source data capture.

  7. Navigate The Early Phases Of Product Development With Ease 6/16/2025

    Early Phase Experts

    As a full-service contract research organization, Southern Star Research has the knowledge, industry relationships and technical expertise to get your early-phase clinical trial up and running safely and efficiently.

    With a broad range of experience delivering Phase 1 Healthy Volunteer, First in Human, First in Patient and Phase 2 trials, we know just how important it is for your asset to succeed in the early development lifecycle. Our experienced team will help you obtain high-quality data that will appeal to future investors, meet the requirements of international regulatory bodies such as the FDA, EMA, PMDA, and Health Canada, and prepare your product for larger Phase 3 and 4 studies, partnerships, licensing, and sale.

    Whatever your clinical trial needs, we can provide a flexible, bespoke solution that will not only meet your regulatory requirements but also position your product for commercial success.

  8. How And Why We Decided To Bring 'Pathways' To Market 3/26/2024

    Over the past year, this author has collaborated closely with a diverse team of clinicians and research experts to enhance Medable's research methodologies across various therapeutic domains.

  9. Intelligent Trials: Design and Execute Faster Trials with AI-Powered Insights 11/19/2024

    Explore how Intelligent Trials leverages the industry’s largest clinical dataset to accelerate enrollment, improve diversity, and provide real-time insights, ensuring efficient, data-driven trial success.

  10. Streamlined Deployment And Patient Data Collection 7/31/2025

    Navigate the inherent complexities, infinite variables, and constant changes that define life-sustaining studies with confidence using a patient-centric platform.