Info Sheets

MERIT’s cloud-based EXCELSIOR software platform enables easy upload of oncology images (CT, MRI, PET) to one secure, validated and FDA-cleared application. This facilitates real-time, trackable, and transparent communication. Learn more in our info sheet.

MERIT is a global clinical trial endpoint services provider offering reliable and attentive expertise in our therapeutic areas. Learn more about what sets MERIT apart in this info sheet.

Gene therapy trials in Inherited Retinal Diseases (IRDs) present unique challenges for biopharma drug developers. Choosing MERIT as your clinical endpoint expert gives you access to solutions based on experience supporting 31 gene therapy trials in IRDs.

What if your company’s early meetings with the FDA to review your preclinical data have indicated a need for ophthalmology safety endpoints in your upcoming non-ophthalmology clinical trial? Discover what your next steps should be in this info sheet.

Many full-service CROs have elected to integrate and use our solutions to manage the imaging and data management elements of their clinical studies. We are thoroughly familiar with the hurdles that CROs may face and can help you proactively address them to meet your customers’ expectations. Learn about the benefits of CRO partnerships with MERIT.

MERIT’s commitment to quality is the foundation of our safe, reliable, and efficient data analysis and management services for clinical trials. Discover the four cornerstones of MERIT services in this info sheet.

 MERIT’s ophthalmic expertise and cloud-based imaging platform performed a crucial role in a global Phase III Wet AMD study. Take a look at a few key metrics from our case study.

ETDRS BCVA has become the gold standard for BCVA testing and plays an integral role in ophthalmic clinical trials. Discover 3 vital aspects of ETDRS BCVA in our info sheet.

What if you could fully-engage sites in every stage of a respiratory clinical trial from startup to conductance to closeout so that your next study completed ahead of time and under budget? Take a look at a few metrics from one of our methacholine challenge bioequivalence studies.

Learn how site support and engagement leads to faster recruitment, better retention, and shortened timelines for respiratory trials.

Why is ISO 27001 certification important? What assurance does it provide? What do sponsors and CRO partners gain from working with an ISO 27001 certified company? Learn the answers to these questions in this info sheet.

MERIT’s customer service approach is unique. Find out how we drive study milestone achievement and increase site engagement.

Any sponsor or CRO managing a drug development program that requires imaging endpoints knows the challenges that can arise. To address these challenges, you need a clinical endpoint expert. Here are four reasons why.

MERIT represents a reliable alternative in respiratory service providers, offering agile and attentive centralized spirometry expertise.

The right centralized spirometry partner can support your team and help you find efficient, reliable solutions for respiratory trials.

Keep an eye on these 5 common imaging study challenges as you plan your future trials.

Download our checklist for reference when selecting a DCT technology partner.