Delivers the highest quality imaging endpoint data, built on decades of experience supporting worldwide clinical trials
Customizable to meet all randomization and trial supply management (RTSM) needs and backed by the industry’s most experienced system designers
With reliable submission planning, publishing, and registration management capabilities
Delivers a superior user experience and improves data accessibility by streamlining clinical trial data collection and reporting in one easy-to-use platform
Combines trial technology innovation, drug development expertise, and business process optimization so users can plan, administer, and track every aspect of clinical trials from start to finish.
Calyx is the clinical research and regulatory solutions provider most relied on for solving complex challenges in clinical development. We couple our 30 years of experience with innovative technology to deliver clinical trial solutions that improve efficiencies and capture the highest quality data to help the global bio-pharmaceutical industry bring much-needed treatments to patients, faster.
Our Difference is
Over the course of three decades, you rack up a lot of experience. Don’t trust your trial to anyone. Rely on Calyx’s experience to help you meet your development goals.
DRUGS TO MARKET
BREAKTHROUGH THERAPY APPROVALS
Clinical and Regulatory Expertise
Makes a Difference
At Calyx, we’re committed to solving complex problems smarter. To do this, we employ the brightest scientific, technical, and regulatory experts whose experience is unmatched in the industry.
By combining this depth and diversity of expertise with state-of-the-art clinical research and regulatory technology and 30 years of experience, the Calyx team behind your solution explores issues from every angle, uncovers optimal solutions, and delivers high-quality data and regulatory compliance on time and on budget.
Global Support and Presence
Calyx is a clinical trial services company with a global footprint.
With global headquarters in Nottingham, UK and many other offices across Europe, America, and Asia, we’re on the ground wherever your studies take place. Our people understand the geographic and cultural challenges your study faces, support your teams and sites in local languages, and seamlessly deliver eClinical and regulatory services to drive the success of your worldwide trials.
Learn the Calyx Difference
Our expertise is in overcoming challenges that affect clinical trials.
I am very impressed with the Calyx Medical Imaging team who have been incredible collaborators in helping us to advance our lead program. We especially appreciate the team working on tight timelines to help us meet our study start initiation goals. Given that we are a small company, we rely on our collaborators, and the team at Calyx works seamlessly beside us to help us advance our development programs. I look forward to continuing our partnership!
Alicia Herr, PMP
We would like to thank the Calyx Medical Imaging team very much for your contribution to this wonderful (oncology) study outcome. Without you, this (marketing authorization) would have never been possible.
Top 10 Global Pharmaceutical Company
A big thank you to the Calyx Medical Imaging team. This (approval) is also your accomplishment, and you should be very proud of the work you have done to make this possible. More approvals to come!
Global Trial Manager
We relied heavily on Calyx’s IRT expertise and followed their recommendations for overcoming our studies’ challenges, resulting in a solution that perfectly met our RTSM needs for two complex gout trials.
We’re pleased to partner with Calyx and are confident that our customers will benefit from the scientific, medical, and clinical expertise they have honed during their 30 years of delivering reliable eClinical solutions to the clinical development industry.
We chose to partner with Calyx due to their tenured scientific, medical, and technical teams who possess a depth and diversity of experience in providing reliable data outcomes.
Calyx has deep technical expertise in various tumor response criteria, imaging modalities, image collection logistics, data management and regulatory requirements. They gave ArriVent invaluable advice during protocol and charter development. This is coupled with a team of world-class highly specialized independent radiologists, imaging scientists, project managers, medical writers, a very efficient budget and contract group as well as superb internal processes and systems all of which contributed to a very smooth program kick-off for our lead molecule.
Join our growing team and take advantage of the many benefits we offer. Find the position that’s right for you and contact us to learn how you can advance your career while making a difference for patients around the world.