Obesity Services & Products

  1. Central Laboratory Services For Multi-Site Studies 4/28/2026

    At DVCR, our Central Laboratory Services are built for multi-site studies, combining customizable kits, next-day results and real-time shipment monitoring to keep every site aligned and on schedule. Backed by dedicated client teams, a comprehensive Central Lab Manual and rapid-response testing, we deliver the flexibility and speed your studies require.

  2. Trial Enablement Solutions 4/14/2026

    Digital health technologies have the potential to transform clinical trials, yet without careful planning and support, their implementation can increase site burden and jeopardize data quality.

  3. Patient Retention In Clinical Trials And Recruitment Support 4/9/2026

    Accelerate clinical trials with expert patient recruitment strategies delivering faster enrollment, lower dropout rates, and better outcomes.

  4. Post-Marketing Studies And Real-World Evidence Clinical Trials 4/9/2026

    Your trusted partner for decentralized post-marketing surveillance clinical trials and real-world evidence collection. Point-of-need accessibility. Proven compliance.

  5. Drug Safety And Pharmacovigilance Services 4/2/2026

    Navigating drug safety in the era of innovation-driven medicine

    The focus on drug safety and pharmacovigilance has never been more intense. Patient safety remains paramount throughout a product's lifecycle, even as sponsors and marketing authorization holders (MAHs) face increasing complexity in managing safety data. This complexity stems from huge volumes of data generated from scores of diverse sources, much of it rapidly expanding unstructured data. Innovation-driven medicine is a key factor. These dynamics are reshaping the landscape of drug safety, presenting both challenges and opportunities for innovation in pharmacovigilance practices.

  6. AI-Powered Workflows: Accelerating Trial Execution 4/1/2026

    What can 22,000 people with an AI-mindset accomplish?

    Speed without shortcuts

    AI in clinical development at Parexel enables our teams to surface predictive insights at every stage, reducing protocol risk, study delays, and costly trial amendments.

    Parexel's approach to AI in clinical development is built on the Precision Pathway, a strategic operating model that embeds AI across the full trial lifecycle. AI empowers our teams at critical decision points to:

    1. Simplify complex tasks to accelerate timelines: AI capabilities are delivering up to 50% cycle time reductions in IND submission generation.
    2. Apply insights with agility to enable better decision-making
    3. Enhance data handling to drive first-time quality through content generation and workflow automation
  7. Oncology Clinical Trial Experts For Complex Trial Design 3/31/2026

    Complex oncology trials require deep science, regulatory expertise, and coordination. See how integrated teams and adaptive designs speed startup, protect patients, and scale.

  8. Streamline Data Entry And Boost Clinical Trial Efficiency 3/26/2026

    Automate data collection, maximize resource utilization, and increase trial capacity.

  9. Regulatory Affairs 3/25/2026

    In today’s clinical environment, navigating regulatory complexities isn’t optional — it’s essential.

  10. Medical Monitoring 3/25/2026

    Every clinical trial relies on one critical constant: protecting patients while preserving data integrity.