Our industry-leading eRegulatory system, RealTime-eDOCS, is streamlining the way sites, sponsors and CROs manage regulatory documents. Sites are now easily managing all of their study records electronically from study startup to archive while maintaining inspection readiness during the entire process.
eRegulatory Document Management at its Best
No matter your situation, we have an eDOCS solution that fits your needs!
Stand-alone RealTime-eDOCS System: The stand-alone system is the perfect complement to existing research site systems. Not only is this solution cheaper than the competition, no other eRegulatory platform can match its features
CTMS-Integrated: Are you an existing customer of RealTime-CTMS? Awesome! Activate RealTime-eDOCS and experience the first eRegulatory solution fully integrated with a robust clinical trial management system. Additional features include ICF tracking, in-system notifications and single sign-on between systems (no need for extra usernames or passwords).
RealTime-eDOCS Enterprise: Are you managing a site network? No problem. We have you covered with our enterprise system. RealTime-eDOCS Enterprise allows you to easily manage electronic records for multiple studies across multiple sites.
eDOCS Versus the Competition
Even with all these extra features, RealTime-eDOCS still cost much less than the competition!
No Annual Storage Fees. Annual storage fees can become a heavy financial burden at the end of each year.
No Obligation to Pre-Purchase Studies. Don’t let the competition lock you into contracts.
The First eRegulatory System to Go Mobile
- Fingerprint technology for eSignatures
- Refer Patients to Your Studies
- Manage Your Signatures
- Navigate eRegulatory Files
- Manage Your Contacts
All of your records in the palm of your hand.
Download our Mobile App
View study documents, refer patients, sign documents with your fingerprint and more!
WHAT CAN DO FOR YOU?
Allow site users to access and manage regulatory records remotely, making travel between sites unnecessary.
Allow remote monitoring which adds value to sponsors and reduces their travel time and costs.
Set expiration dates for CVs, licenses and certifcations.
Save time and money spent printing, gathering handwritten signatures, filing, scanning, and mailing between sites and sponsors.
Facilitate inspections, audits and study record requests with the FDA, sponsors, and IRBs.
Standardize and centralize eRegulatory binders in one secure location for quick and easy access.
Eliminate paper-based regulatory binders and storage costs.
Allow sites to implement ICF tracking on all subjects within a study.
Increase efficiency using electronic signatures.
Improve collaboration between investigators and sponsors.
Accelerate study start up processes.
eSOURCE has more features, greater scalability, and CTMS integration, all at an affordable price.
Automatically send appointment confirmations and reminders to all your patients
Pay Stipends instantly with this fully integrated payment system. Save time and money
Quick and easy access to study or subject information utilizing simple and intuitive navigation