Clinical Technologies Solutions

  1. Unified, Integrated eClinical Research Solutions 1/16/2024

    Facilitate efficient digitalization and optimization of clinical trials that meet the unique needs of small and mid-size biopharma organizations with the Signant SmartSignals Unified Platform.

  2. Patient Data: The Backbone Of Your Clinical Trial

    In clinical trials, data capture is typically centered around patients’ experiences with a drug. See why electronic clinical outcome assessments (eCOAs) are essential to patient data capture.

  3. Why Leading Cancer Research Centers Trust OpenClinica For Oncology Trials 7/16/2024

    See eight key reasons why leading cancer research centers rely on OpenClinica to navigate the intricacies of oncology trials and advance the field of cancer research.

  4. 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.

  5. Orchestrated Study Start-Up 10/16/2023

    Learn how the IQVIA Investigator Site Portal reduces activation timelines and eliminates site frustrations by automating processes and providing complete oversight to study teams.

  6. Suite Success For Life Science Organizations 9/13/2021

    Leverage Sikich’s experience gained from dozens of NetSuite implementations for Life Sciences organizations, just like yours, to avoid common pitfalls and pave your way to success.

  7. How To Achieve Timely Migration Of Your TMF 9/18/2023

    This precise, proven methodology delivers a high-quality migration of your Trial Master File to the destination system, typically just 4-6 weeks after receiving all documents from the source system.

  8. Use Our Experts For eTMF Management, Monitoring, And Maintenance 3/14/2023

    IQVIA eTMF Expert Services provide on-demand resources to help manage, monitor, and maintain eTMFs. Dive into the ways these services can improve productivity and ensure compliance.

  9. Data Monitoring Committee (DMC) Services 7/23/2024

    Let us build and manage your data monitoring committee or data safety monitoring board, ensuring oversight and the highest standards of data integrity and participant safety throughout your study.

  10. 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.