Real-time visibility into every consent, so you and your sponsors stay aligned from day one.
Delays in signed or missing ICFs can stall enrollment and increase the risk of 483 citations. The Clinical.ly eConsent tool offers complete transparency and control while giving participants the freedom to sign anytime from any device, making enrollment faster, easier, and more convenient for everyone.
Seamless, effective, and compliant – these are just a few of the words that perfectly describe Clinical.ly’s eConsent.
Participants may review and sign the ICF from the comfort of their homes or in the office via their mobile devices.
Improve operational efficiency and get back the time lost chasing down the appropriate ICF and double-checking that your participant is signing the correct version.
The ability to grant remote access to external monitors improves efficiency by freeing site personnel from needing to allocate time hosting on-site monitoring visits.
Our state-of-the-art security puts you in control to delegate uploading new ICFs, versioning prior copies, disseminating appropriate versions to study participants, and gathering consent forms.
Rest assured that your participants are signing the latest ICF version, and your Sponsor and IRB will accept the electronically signed consent form.
Our eConsent comes standard with Clinical.ly Research Suite™ or may be utilized as a standalone product.
“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
