Clinical Trial Solutions
CROs and Calyx. Together at last.

Leverage the experience of an industry-leading eClinical solutions provider to deliver advanced technology and proven services that drive success for you and your customers.

Deliver more. Go Calyx.

Let Calyx’s scientific, technical, and regulatory experts become an extension of your team and deliver the eClinical solutions your customers know and trust.

Although the name is new, Calyx’s solutions have been proven time and time again. Calyx brings nearly 3 decades of industry experience, deep clinical expertise, and a focused investment in advanced technology to deliver solutions that overcome clinical development challenges and get treatments to market sooner.

Calyx’s solutions have been used in over 25,000 trials and have supported more than 250 new drug approvals, including 50% of recently approved breakthrough oncology therapies.

Learn how Calyx can help you deliver more value with the industry’s leading Medical Imaging, Randomization & Trial Supply Management (RTSM or IRT), CTMS, EDC, and Regulatory Information Management(RIM) solutions to your existing and future customers.

Deliver more. Go Calyx.

Let Calyx’s scientific, technical, and regulatory experts become an extension of your team and deliver the eClinical solutions your customers know and trust.

Although the name is new, Calyx’s solutions have been proven time and time again. Calyx brings nearly 3 decades of industry experience, deep clinical expertise, and a focused investment in advanced technology to deliver solutions that overcome clinical development challenges and get treatments to market sooner.

Calyx’s solutions have been used in over 25,000 trials and have supported more than 250 new drug approvals, including 50% of recently approved breakthrough oncology therapies.

Learn how Calyx can help you deliver more value with the industry’s leading Medical Imaging, Randomization & Trial Supply Management (RTSM or IRT), CTMS, EDC, and Regulatory Information Management(RIM) solutions to your existing and future customers.

We get you. Really.

At Calyx, we have a long history as part of a CRO, so we know how a CRO functions, the challenges you’re up against, and the importance of keeping your customers satisfied. This inside knowledge affects every aspect of our CRO relationships and makes us more efficient and easier to work with.

Driven by our dedication to adding value to your customer relationships, we adhere to a strict Code of Conduct that’s centered on our unrelenting commitment to confidentiality.

Put Calyx experience to work for you
Partnering for success.

Calyx’s partnership program, “ACTIVATE Solutions for CRO Partners” is designed to improve short-term and long-term alignment between our organizations so that together we can better support clinical development pipelines.

- Calyx’s renewed focus – priority investments in already industry-leading technology

- A symbiotic relationship – increased industry focus and reduced long-term costs

- Calyx’s unique position of understanding your challenges, based on our history as part of a CRO

- Access to market-leading subject matter experts

- Structured onboarding process with training and certifications

- Increased accountability through streamlined issue resolution and innovation

- Improved client satisfaction and study compliance

Learn how you can better meet the broad and fluid requirements of your many different clients, programs, vendors, and technologies by partnering with Calyx today.

Your customers rely on you. You can rely on Calyx.

How can you deliver more value to your customers? Couple your comprehensive services with Calyx’s proven eClinical solutions to improve clinical trial efficiencies and accelerate their clinical development programs.

In addition to improving quality and compliance through consistent regulatory rigor and globally dedicated support, Calyx’s tech-enabled services like system implementation, integration, and protocol review help you streamline study execution and data delivery, so your customers get to market faster.

Library
Behind the Breakthrough
Earning the FDA’s prized Breakthrough Therapy designation is just the beginning of the race, one that likely requires the use of an imaging surrogate for preclinical evidence and accelerated approval.
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Driving Trial Efficiencies with Effective CTMS
A leading pharmaceutical company with more than 30 development projects in clinical trials worldwide is relying on Calyx CTMS to make robust, data-driven decisions that ensure patient safety.
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Reviewer Performance Monitoring in Blinded Independent Central Review Setting
This white paper reviews how the assessment of imaging data in support of surrogate endpoints by an independent entity reduces evaluation bias and improves assessment consistency in clinical trials.
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Optimizing Regulatory Information Management
With an effective Regulatory Information Management (RIM) system, you can learn from your experiences, anticipate regulatory requests, and ultimately, get treatments approved faster to help improve people’s lives.
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