Clinical trials simplified.
Hundreds of organizations of all sizes - from small consumer brands to large pharmaceutical companies - use Citruslabs to bring their clinical trials and research studies to life.
Full-service digital CRO
We designed a clinical trial process so easy, you might actually enjoy doing it.
Citruslabs brings together everything that is required to conduct and manage successful clinical trials, from study design to trial completion. We help you design your study, write the protocol, submit to IRB, recruit and manage your patients (or healthy volunteers) as well as collect and analyze the study data, offering you a hands-off, carefree approach to your clinical studies.
Citruslabs’ products power clinical research for hundreds of organizations of all sizes, from consumer brands, offering supplements and skincare or cosmetic products, to biotechs and pharmaceutical companies that bring new investigational drugs and treatments to market, to academic institutions. We support virtual trials, hybrid models and site-based studies.
How we can help your clinical trial come to life
Designed to accelerate your research from start to finish
Put your clinical trial process on autopilot with Citruslabs. We provide you with a full suite of products to conduct your clinical study. Regardless if you are looking to conduct your studies fully virtual, follow a site-based approach or mix it up with a hybrid clinical trial, we can help you!
Study materiel development
Clinical Protocol creation
Clinical study report
Why study sponsors love us
Faster, smarter, more cost-efficient clinical studies
Through technology and automation, we are setting new standards for clinical research and help our clients run faster and more cost-efficient clinical trials. Costly delays and mind-blowing budgets are a thing from the past. Plus, our platform allows you to offer a better patient experience and receive a higher quality of data in return.
200+ clinical trials served
30+ indications covered
95% higher patient satisfaction score
The smartest way to find & retain participants for your study
Enrolling the right candidates on time has historically been a challenge for many clinical trials. We are committed to recruiting your study participants in a certain timeframe and in a cost-efficient way. Retention & study adherence is part of our DNA and our excellent retention numbers speak for themselves.
Frictionless data capturing & analysis
Our optimized data capturing is reliable and offers our clients a unique dataset to show the efficacy and safety of your products, drugs and medical devices. Regardless if you are following a centralized or decentralized approach to your clinical studies, you have 24/7 access to your data, which is consolidated in our easy-to-use platform.
Efficient, transparent study set-up and management
We provide you with a seamless experience from study start-up to completion. Our vast network of patients and healthy volunteers allows us to include unique insights into your study design and beyond. Monitoring, tracking and analyzing trial progress in real-time has never been easier; and starting your study has never been quicker.
A technology-first approach to clinical research
Study startup that takes weeks, not months
Citruslabs has the expertise and insights to make designing your clinical study effortless. We are involving patients in the process from the start to set your study up for success.
Access to world's largest patient data base
With over 25 million patients and healthy volunteers in our database, we fill your clinical trial in days, not months. Participants are educated on your studies and excited to make a difference.
Study execution driven by software
Through Citruslabs’ clinical trial platform you can capture data from multiple sources. Regardless if your trials are site-based, hybrid, or fully virtual, we got your back.
Ready to get started? Get in touch today and find out how we could partner with you.
We bring together everything that’s required to run successful clinical trials. Citruslabs products power research from study design to patient recruitment to trial completion.
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