Criterium, Inc. is a full-service, global CRO (contract research organization) offering a unique mix of high-quality clinical research services, and real-time data acquisition and supervised by information management specialists. We use personalized communication processes to manage a clinical trial from initial planning to approval, on time and on budget. Founded in 1991, the Criterium team provides a high level of therapeutic expertise, high-quality clinical development services, and highly efficient processes to pharmaceutical, biotechnology, and medical-device companies.
Using innovative products to improve efficiencies, Criterium's staff is able to handle large-scale clinical projects while providing the personal attention lacking in larger CRO's. Our centralized clinical trial data management environment provides a compliant, standardized methodology for processing, validating and presenting real-time information to clinical trial management and monitors. Using proprietary Interactive Voice Response System (IVRS) and Web Board Reporting (IWRS), Automated Fax (FAX), Electronic Data Capture (EDC) and online data reporting for over a decade , Criterium has developed and managed registration, randomization, study drug tracking, electronic patient diaries (TeleDiaryTM, Criterium's IVRS/IWRS ePRO application) and real-time data capture and reporting. At Criterium we manage the data EVERY DAY for timely decision making, rapid data editing and on-time delivery of the final deliverable – usually a final study report.
At our foundation, Criterium clients receive:
- Quality Solutions that meet or exceed the clients' expectations for the entire clinical-research process, from initial planning to approval, which can be customized to fit each client's specific needs. Data transmitted centrally are reviewed by teams that work closely together, every day, at the same location.
- Reduced Costs by transforming "traditional" monitoring tasks to centralized monitoring through workflow using proprietary technologies -- and SaaS -- without the additional purchase of expensive computer hardware and software.
- Accelerated Timelines through placement of studies at sites based on their ability to enroll and evaluate valid patients while still using site friendly proprietary tools that do not burden their staff for more rapid data collection: sites and patients enter data directly into the study databases for daily monitoring. Our database of international sites capitalizes on seasonality factors where appropriate.
Criterium has offices in New York, California, Florida, South Africa, India, Russia, and Canada with representation in Israel and Western Europe to provide personal service to clients throughout the world. All are supported by modern standardized technologies that have been developed and are maintained in our New York headquarters.
We have earned a worldwide reputation as a leading CRO, with successful experience in all phases of clinical research and across major therapeutic areas. Because of our emphasis on being agile, our people, processes and technology combine to meet our clients' unique and changing needs.
At Criterium, who we are, what we do, and how we do it are centered on our service reputation: an uncompromising "Always Delivers" attitude in everything we do.
Get To Know Us!
Visit http://www.criteriuminc.com/ for further information.
Clinical Trial Design, Clinical Trial Monitoring, Data Management, Efficacy Studies, Electronic Data Capture, Project Management, Randomization (Automated/Centralized/Vocal Computer), Regulatory Document Preparation, Remote Data Entry, Trial Management
358 Broadway, Suite 201
Phone : 5185830095
Internet : www.criteriuminc.com
Email : BusDev@criteriuminc.com
Contact Person : Claire Wynters