Featured Products

1. Your Trial Is In Jeopardy. Time Is Critical. 10/15/2025

   Expert ophthalmic teams rescue clinical trials with stabilized studies, nationwide coverage, and eye assessments, helping protect endpoints and regain timeline control quickly.

2. Compliance And Adherence 4/6/2016

   Compliance and Adherence Packaging can play an effective role in maximizing patient compliance and adherence by helping to address core challenges through the use of support tools. PCI provides insightful and multifaceted solutions for addressing patient compliance and adherence for clinical investigational medicines as well as commercial applications.

3. 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.

4. Contract Stick Packaging Services For Pharmaceutical And Nutraceutical Applications 5/19/2015

   Ropack recognizes that the unique design of stick-pack offers multiple benefits – for pharma and natural health products as well as to consumers.

5. GMO Solutions 6/27/2023

   Novotech initiated the first national, privately owned, commercial Institutional Biosafety Committee (IBC) in Australia, successfully accredited by the Australian Office of the Gene Technology Regulator (OGTR).

6. 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.

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. 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.

9. Multitherapeutic Limitations: Knowing How To Choose The Right Resource 7/20/2021

   Chief medical officers looking for outsourcing services on a study are often fed lines from large CROs on how they can provide individuals with multitherapeutic backgrounds.

10. MRN Technologies 11/22/2024

    Our research is powered by MRN owned, regulatory-approved and validated eClinical software systems. Our technology can be used at-site and at-home enabling fully integrated data through any clinical trial.