Central Laboratories Products/Services

1. 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.

2. Electronic Data Capture (EDC) System: Leverage Flexibility And Speed 8/11/2025

   Neither traditional nor hybrid clinical trials can operate on rigid EDC systems.

   They require flexible data collection systems that support protocol amendments without downtime and accept mobile data without hassle. As a cloud-native solution, TrialKit bends to accommodate mid-study changes. And as the first full-featured EDC platform available as a native mobile app, TrialKit flexes to meet the demands of traditional, hybrid/decentralized, and completely remote clinical trials.

   Give your team the freedom to build, deploy, and manage their studies, their way—weeks faster than with rigid EDCs and for a fraction of the cost of the major players.

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. Revvity Signals Software Risk-Based Monitoring Solution 8/28/2017

   The Revvity Signals Software Risk-Based Monitoring Solution is the most effective way to leverage data-driven insights to optimize site performance while improving patient safety.

5. Modern ePRO/eCOA: Craft A Unified Digital Patient Experience 8/29/2024

   It’s about time.
   Modern ePRO/eCOA.
   Solved.

   Don’t wait a lifetime to launch a study that’s just “good enough”. Build and design a data collection experience that patients and sites will love to use.

6. TrialKit: Your Comprehensive Solution For Non-Interventional Studies 4/5/2024

   Elevate Your Clinical Research Data Collection

7. 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.

8. Data Management: Turning Data Into Insights 7/31/2025

   Turning Data into Insights

   At Catalyst Flex, we understand that clean data is the foundation of successful analyses. We are an accredited Medidata Partner and certified study builders in multiple platforms.

9. A Single Digital Experience Participants Will Love 8/29/2024

   Experience higher data quality, retention and participant compliance by providing a truly engaging experience from data submission to reminders, appointment management, telemedicine and more -- from the phone, tablet, or desktop.

10. Digital Transformation Services 8/29/2024

    Enabling organizations of all sizes to transform their business through better use of technology.