Obesity Services & Products

  1. End-To-End Biostatistics In Clinical Research 7/31/2025

    Comprehensive Solutions to Drive Efficient Trials

    Catalyst Flex delivers end-to-end biostatistics in clinical research solutions to drive efficient, high-quality trials. We offer:

    • Customized data solutions and innovative trial designs
    • Flexible engagement models, from a single expert to full-function teams
    • Consistent, submission-ready deliverables from our dedicated biostatisticians and statistical programmers

    Our experienced Catalyst Flex staff are committed to seamlessly embedding with your team to meet every study objective.

  2. eCOA: Delivering High-Quality Patient Data 7/31/2025

    Purpose-built with users at the center to make it easier and more efficient to get quality patient outcomes data for submissions and approvals.

    Collecting quality data on patient outcomes is often one of the most important parts of a clinical trial. It is also challenging, and many eCOA solutions make it feel even more difficult with complicated processes, lack of questionnaire reusability, slow set up, and difficult to use tech.

  3. Computer Systems Assurance And Validation 7/22/2025

    Computer System Validation to cover all your GMP, GLP, GCP, and QA/QC software applications. CompliancePath currently has 30+ active projects globally supporting clients in CSV/CSA compliance.

  4. Gain Instant Access To HEOR Education With On-Demand Programs 7/15/2025

    The ISPOR Education Center provides instant access to Health Economics and Outcomes Research (HEOR) education with on-demand programs delivered through a personalized, powerful, and flexible learning platform. Working at their own time and pace, individuals can drive their professional development by growing their knowledge and skills with topical, relevant, and innovative course curricula.

  5. What If Your Study Portal Actually Helped Patients? 7/15/2025

    Patients shouldn’t have to jump through hoops. Discover an innovative portal that lets them handle travel and reimbursement directly—securely, simply, and without extra calls to the site.

  6. An Easy-to-Use Analytics Platform For Clinical Trial Vendor Selection And Management 7/1/2025

    ClinAI helps you centralize RFPs, budgets, and vendor data—so you can select the right partners, manage change orders, and keep your studies on track.

  7. Document Review Integrations And Technology Partners 6/18/2025

    At Ideagen, we're committed to empowering seamless collaboration and enhancing your document review process. Through strategic alliances with leading technology providers across the life science industry, we offer integrations that amplify the efficiency and effectiveness of your workflows.

  8. 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.

  9. Clinical Operations: From Study Feasibility And Recruitment To Trial Monitoring And Quality Assurance 6/16/2025

    Our Approach

    At Southern Star Research, we have extensive experience across all aspects of clinical operations and a wide range of therapeutic areas. We specialize in providing flexible, high-quality, and custom solutions that help you deliver regulator-ready data on time and at a predictable price.

    As a large proportion of our clients are geographically dispersed, we understand how important it is to be able to trust that your CRO is working in your best interests. That’s why we pride ourselves on building strong, transparent, and close relationships with our clients.

    Our team of experts will guide you through the clinical trial process using a proactive and collaborative approach, ensuring that your stakeholders are always informed, in control, and confident throughout the journey.

  10. 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.