Obesity Services & Products

  1. Enable Value-Based Evaluation Of Medicines 3/28/2025

    Trial@home, CHDR’s dedicated strategy for off-site clinical trials, enables investigators to collect information as trial participants go about their day to day activities.

  2. Empower Your Research Sites With A Full-Service Marketing Solution 3/27/2025

    Built for Sites, Not Just Sponsors

    Too many recruitment vendors focus solely on the sponsor’s bottom line, leaving sites stuck managing clunky spreadsheets, manual tracking, and outreach tasks without the infrastructure to scale.

  3. Commercial Alerts: Now Available With EHR, Claims And Prescription Data 3/27/2025

    Identify & engage healthcare professionals (HCP) treating eligible patients—in near real-time

    Timely physician engagement is critical to therapy adoption. Quest Diagnostics combines near real-time lab data with other data sources including EHR, claims and prescription data to help pharmaceutical teams identify and connect with physicians managing eligible patients at key decision time point in the patient journey.

    In today’s competitive pharmaceutical landscape, ensuring that physicians receive timely, relevant information about new therapies is essential. Quest’s unique combination of industry-leading deidentified lab data, enhanced with claims, prescription (Rx), and EHR insights, allows pharma teams to refine targeting, optimize engagement, and drive better patient outcomes.

  4. A QMS Software That Enhances Operational Excellence 3/24/2025

    Ideagen Quality Management is a modular SaaS solution designed with the needs of quality managers in mind. Trusted by more than 6,000 customers worldwide to digitalize their quality management processes and comply with industry standards.

  5. Regulated Document Review 3/24/2025

    Enables secure real-time document review, co-authoring, and redaction in order to shorten the document review process by up to 65%.

  6. eCOA And ePRO Solutions For Clinical Trials 3/10/2025

    Planning to launch a patient-centric decentralized clinical trial? Give your clinical trial patients an app that makes it easy to participate—from anywhere at any time.

    Simplify clinical trial participation with an integrated eCOA and ePRO solution

    TrialKit’s electronic clinical outcome assessment (eCOA) and electronic patient-reported outcomes (ePRO) platform integrates with all currently available wearables, mobile operating systems, and web applications. Whether you collect data in the clinic, with provisioned devices, or take a bring-your-own-device (BYOD) approach, you can count on seamless data sharing and efficient study execution.

  7. Make Participating In Your Clinical Trial Easier Than Ever 2/20/2025

    The success of clinical trials depends on patient participation.

    But patients and caregivers need reliable support first.

    Being part of a trial is often nuanced and time-consuming. Archaic travel, antiquated payment processes and card fees are not only frustrating, but can also chip away at the reimbursement funds participants are owed.

    This isn’t what you want for your participants, but you haven’t had a better choice. If we have the technology to make things better, we should. So we are.

    Mural Link is the clinical research industry’s first participant management platform, designed to meet the needs of modern-day participants, help them enroll and remain in a trial, and reduce the administrative burden for sites.

  8. Ergomed's Risk-Based Quality Management 2/6/2025

    Ergomed’s Meticulous Risk-Based Quality Management Approach

    As a pioneer in providing comprehensive support for your clinical research, Ergomed champions an innovative Risk-Based Quality Management (RBQM) approach. This forward-thinking strategy ensures the highest patient safety standards, regulatory compliance, and data reliability. Ergomed’s proactive approach to managing clinical trials tackles clinical research complexity head-on.

  9. Targeted Source Data Verification 2/6/2025

    Ergomed’s Risk-Based Clinical Monitoring and Source Data Verification Approach for Data Integrity

    Ergomed ensures the highest data integrity and patient safety standards through our risk-based clinical monitoring and Source Data Verification (SDV) practices. SDV is a critical process in clinical trials that ensures the data collected are accurate, complete, and verifiable against the source documents. We compare data entered into case report forms or electronic data capture systems with the source data to confirm their accuracy and reliability.

  10. Ergomed's Patient-Centric Focus Drives Our Team 2/6/2025

    Ergomed places patients and their care partners’ needs at the core of our services. We strive to build empathetic relationships with patients and their care partners, not just during the trial but also before and after. Our team provides personalized support, aiming to alleviate the burden of study participation. Ergomed and our trusted partners are deeply committed to bringing lifesaving treatments to patients.