Drive better decisions faster with real-time data at your fingertips.
Our technology innovations target rapidly evolving clinical trial models, in support of virtual trial data collection, IRT, RTSM, remote monitoring, eCOA/ePRO, reporting, communication, registries, and real world data collection platforms.
Virtual Clinical Trial Solutions and Patient Engagement Solutions
The pandemic has catalyzed changes in the way clinical trials are conducted and sponsors are turning to virtual clinical trial solutions, decentralized clinical trial recruitment, and remote patient engagement solutions. At IVRCC, we’re clinical trial technology experts who specialize in bringing the trial to patients with decentralized clinical trials, ePRO/eCOA, and BYOD to achieve high compliance from subjects.
Our agile innovations for virtual clinical trial success:
Subject Screening, Registration & Randomization
IVRCC implements and tracks subject screening, registration and randomization with immediate access to key subject metrics, enabling critical decisions to be made based on trial progress towards project goals.
Clinical Trial Material Management
IVRCC’s automated systems enable real-time management, with blinded and unblinded reporting, of clinical trial material dispensation, inventory and re-supply for all stocked locations.
Electronic Patient Diaries and ePRO Solutions
IVRCC’s user-friendly Electronic web & voice systems provide access to diaries, surveys and QofL questionnaires, resulting in high compliance for timely collection of accurate subject reported outcomes.
eClinical Integration
IVRCC’s integration technologies offer multi-directional and transactional and/or scheduled data sharing between any eClinical applications.
Patient Recruitment & Outreach
IVRCC’s Interactive Voice and Web Response Systems are powerful tools at every stage of the recruitment process.
Real-Time Reporting
IVRCC provides real-time data tracking and management of patient registration, automated randomization, and diary compliance, which results in better clinical trial management.
Data Collection & Compliance
Automated triggered alerts and notifications minimize the burden on site personnel to personally keep subjects fully engaged in completing diaries and questionnaires.
Custom Design & Clinical Expertise
The combined experience of the IVRCC staff is well over 100 years, with Interactive Voice/Web Response experience in 200+ clinical trials.
We work with top 10 Pharma companies, large academic institutions, innovative specialty biotechnology companies, large and small CROs, medical device companies, commercial service companies, healthcare groups, Oncology consortia, and EDC technology providers around the globe. Our application is highly scalable and able to accommodate small individual site IIT studies to large multi-national trials with unlimited numbers of sites, subjects, and modalities, with varying complexities.
- Pharmaceutical Companies
- Biotechnology Developers
- Medical Device Firms
- EDC Vendors
- Contract Research Organizations
IVR Clinical Concepts has deployed subject registration, randomization, trial supply management (RTSM) and ePRO/eCOA clinical services for numerous global projects and studies in multiple Therapeutic Areas.
- CNS & Neurology
- Oncology
- Endocrinology
- Hematology
- Gastroenterology
- Otolaryngology
- Infections & Infectious Diseases
- Dermatology
- Cardiology
- Orthopedics
How we’re different:
With 30 years of experience, we have deep knowledge of data collection.
We’re adept at addressing unique clinical trial technology challenges across many therapeutic areas.
We think outside the clinical trial box.
We build custom applications without the custom cost. Our flexible platform delivers technology solutions to solve your data problems at any budget.
We’re all about the experience.
We bring the trial to patients with decentralized clinical trials, ePRO/eCOA, and BYOD to achieve high compliance from subjects. Our dedicated team continuously monitors and supports your study, from IVRCC build to close-out.
We’re dedicated to QA.
Our dedicated QA department stays on top of validation procedures, regulatory compliance, and all quality assurance factors to verify data security, privacy and integrity.
Real-time data means real-time decision making.
Having real-time study knowledge at your fingertips gives you the ability to adapt and adjust, increasing trial speed and reducing trial cost.
Our service doesn’t end at launch
Our dedicated team of professionals is always available with 24/7/365 support to ensure all needs are met quickly and completely from start to finish.
Custom, modular, and configurable
virtual clinical trial solutions
Speak to an expert today: 561-789-4890
Together, let’s make your next project a success.
Nancy Hudak
Business Development Analyst
561-789-4890
