Streamline every aspect of your research—from startup to closeout—with one unified platform.
As a Clinical.ly client, you’ll harness powerful, purpose-built technology designed to simplify every aspect of site operations. Our integrated suite helps you run more studies with less effort- accelerating startup, improving compliance, and reducing data entry errors. With Clinical.ly, your team can focus on what matters most: delivering high-quality research and exceptional participant care, without adding administrative burden or extra staff.
Explore the advanced features of our best-in-class electronic regulatory binder. Simplify document management, improve compliance tracking, and keep every trial audit-ready from day one.
Experience the most intuitive and efficient electronic source solution on the market. Capture, review, and verify data seamlessly while reducing errors and eliminating redundant workflows.
Deliver a compliant, seamless electronic consent experience for participants. Simplify document handling, ensure version control, and streamline approvals for faster study startup.
Purpose-built for research sites, our electronic signatures management tools ensure secure, compliant, and efficient workflows for every stakeholder in your trial.
Seamlessly pay study participants through Clinical.ly. Minimize administrative effort while improving participant satisfaction and study retention.
Achieve real-time financial visibility and audit-ready compliance. Eliminate manual tracking and ensure every dollar is captured.
Streamline every aspect of site operations with structure, visibility, and efficiency. Simplify scheduling, resource management, and daily workflows to deliver exceptional research and patient experiences.
Leverage our Research Suite to scale your studies, increase efficiency, reduce mistakes, & stay compliant without requiring additional staff. Our platform becomes smarter with each new study, saving your team valuable time and resources.
Looking to eliminate days of work from your study startup timeline? Let us show you how.
As trials keep evolving in complexity, it is apparent that the same old procedures aren’t keeping up. Inspection findings are much more costly than adopting the right technology, procedures, and best practices. We collaborate closely with clinical trial sites to understand their SOPs and deliver solutions tailored to their unique needs. By integrating with your proprietary workflows, the Clinical.ly Research Suite reduces technology barriers, allowing you to focus on your patients.
Our technology adapts seamlessly to your site’s existing workflows, never the other way around.
Stop wondering if the appropriate tasks were delegated and prerequisite training completed. You no longer need to chase staff and PIs for signatures…
Effortlessly sign and collect electronic signatures while eliminating missed signatures and incomplete forms—saving you and your team valuable time.
Drive enrollment and stay compliant with a fast, frictionless, and easy-to-track informed consent experience.
Pay and reimburse trial participants at the time of their visit using their preferred payment method and ensure a positive experience.
Ensure accurate, timely data capture with enhanced protocol adherence. Automatically validate entries and generate alerts for missing or incomplete data points.
“Clinical.ly Research Suite has saved us so much time and makes regulatory much more efficient. The ability to document training and delegation electronically has played a huge role in improving our workflow.”
Founder & CEO,
Rochester Clinical Research
“We, as a site, love using eRegBinder. As the administrator of the system, I’m impressed with the functionality, level of customization, and quick and efficient responsiveness of Clinical.ly’s customer support.”
Director of Clinical Research,
Suncoast Neuroscience Associates
“Clinical.ly is a prompt service provider who is sincere in their approach and steadfast to continue to develop their platform to meet our needs. We were able to leverage the efficiencies of Clinical.ly Research Suite to facilitate the transition of over 50 trials to a new research location.”
CCRC Senior Director / Co-Owner
Coastal Carolina Research Center
“As a busy research site that has historically conducted over 700 industry clinical trials. Clinical.ly has been crucial to a workforce that is increasingly remote or working within flexible working environments, enhancing our ability to organize our study documents and processing regulatory documents.”
CCRC Senior Director / Co-Owner
Coastal Carolina Research Center
“On January 1st, 2021, we were able to leverage the efficiencies of Clinical.ly Reseach Suite to facilitate the transition of over 50 trials to a new research location.”
CCRC Senior Director / Co-Owner
Coastal Carolina Research Center
“I’m impressed with the operational efficiency we achieved with Clinical.ly’s platform. The ability to sign documents digitally, track expirations, and set up alerts & reminders enabled us to take on more trials while maintaining the highest quality.”
Baptist Health
Center for Clinical Research
“As an academic center, we conduct a myriad of clinical trials, clinical research, and pre-clinical/biomedical research. The use of Clinical.ly Research Suite has simplified our document management, helped streamline our processes, and overall improved our efficiencies.”
Director- Clinical & Aerospace Health Research
University of Central Florida College of Medicine
“Clinical.ly products are user-friendly and intuitive. It is evident that Clinical.ly is committed to the support of their customers’ research sites and the overall advancement of clinical trials.”
Manager, Clinical Research
University of Central Florida College of Medicine
“It is funny that now that Clinically is implemented, nobody wants to sign a paper anymore! Not even our staff! It is definitely saving us a lot of time!”
VP of Quality & Regulatory Affairs
FOMAT Medical Research
Making clinical research an integrated care offering in a national health system requires an efficient, comprehensive software solution that satisfies regulatory requirements while being intuitive and user-friendly for those whose priority is patient care. Clinical.ly checked all the boxes and far exceeded our expectations.
National Medical Director of Clinical Research
Research Division/Program Co-Founder at
Carbon Health
Transitioning from paper DOA, training logs, and overall paper regulatory binders to Clinical.ly (eReg, eDOA, eTraining Logs) improved our site’s efficiency! Our sponsors are pleasantly surprised with the ease of navigating the system and downloading the documents they need.
Can’t imagine going back to paper!
Site Director
AMCR Institute, Inc
Clinical.ly‘s focus on the site-user experience has improved our eRegulatory efficiency and operational output while setting new industry standards. The system’s quality is second only to the customer service provided; I can’t wait to see where GLRI is headed with Clinical.ly on our team!
Director of Clinical Operations
Great Lakes Research Institute
Clinical.ly has been a game-changer for our team! The platform is incredibly user-friendly, making the transition to an electronic regulatory system smoother than imagined. What really stands out, though, is the fantastic customer service. Their support team is always responsive, knowledgeable, and genuinely dedicated to helping us succeed.
President
GNP Research
“Can I just say how wonderful the Clinical.ly people are? Almost anything I ask of them, they try to figure out a way to make it happen, and they respond to tickets within minutes, not in months.”
Tribe Clinical Research
