Obesity White Papers & Case Studies

  1. Disclosure Management System: Build Or Buy? 6/19/2025

    Clinical trial disclosure regulations are tightening worldwide. In order to maintain compliance, sponsors must determine whether to build an internal disclosure management system or buy a solution.

  2. Support For Complex Regulatory Documents 6/19/2025

    The dedicated team of expert writers and editors offer you a wide range of disclosure-related services, including writing, editing, redaction, quality control, and submission.

  3. Completed Clinical Trials Continued To Climb In 2024 6/19/2025

    Data collected in this report reflects a shift toward sustained growth, reflecting rapid advancement in therapeutic areas such as oncology, autoimmune/inflammation, and central nervous system studies.

  4. Data Key In Addressing Patient Recruitment Challenges 6/19/2025

    Explore how a Phase II trial for extensive-stage and previously treated small cell lung cancer overcame recruitment challenges with a data-driven solution designed to surface protocol-matched patients.

  5. How Sponsors Can Drive Success With Central eSource At Investigator Sites 6/17/2025

    Centralized eSource systems enable complex clinical trials to align with key regulatory frameworks, including ICH E6(R3), ICH E8(R1), and 21 CFR 312, to meet the highest standards of GCP.

  6. A Proven Approach To Ensure Scoring Consistency And Endpoint Quality 6/17/2025

    Address inconsistent assessment scoring that masks treatment effects and inflates placebo responses while delivering cleaner endpoint data through standardized scale administration.

  7. Immunohistochemistry In Precision Medicine: From Biomarker To Clinical Trial Assay 6/17/2025

    From preclinical validation to clinical implementation, immunohistochemistry (IHC) is essential in understanding target biology and ensuring drug safety and efficacy.

  8. High-Content Flow Cytometry 6/17/2025

    Flow cytometry is a foundational tool in modern drug development, and its application in receptor occupancy assays has become essential for evaluating therapeutic engagement with disease targets.

  9. Document Collaboration, Controlled 6/17/2025

    Streamline document reviews in life sciences with an innovative platform that ensures accuracy, compliance, and collaboration across teams for managing complex, high-stakes workflows efficiently.

  10. Reimagining How You Bring Life-Changing Therapies To Patients 6/16/2025

    Accelerate your therapy's path to market and create better experiences with the right partner to provide end-to-end Clinical Development expertise.