 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
||||||||||||||||||||||||||
|
|
|
ResearchPoint is a Contract Research Organization offering a global reach with an individualized approach.
The ResearchPoint team consists of members who have some of the
best process, therapeutic and technology expertise you'll find
in CROs today. A more detailed scenerio can be discussed with Stacey
Vesterfelt.
Our continuum model, however, truly sets us apart.
At ResearchPoint, we complement the research and development function of pharmaceutical, biotechnology and medical device companies.
Unlike some CROs, we do not mimic the typical silo infrastructure. Instead, we deliver a more streamlined, cost-effective clinical development process.
At ResearchPoint, we provide the traditional cornerstone services found within our industry.
Unlike some CROs, we excel in managing the entire clinical trial process. By cross-training our team members, traditional monitoring and data management functions are melded together, resulting in a greater sense of responsibility for and ownership of the clinical development process. This provides our customers with comprehensive data quality monitoring. The added benefit of such cross-training is experienced by our customers when utilizing ResearchPoint for monitoring only or data management only projects, but is maximized when ResearchPoint has the opportunity to manage the whole trial.
At ResearchPoint, we offer data solutions for early- and late-phase
clinical trials, using conventional paper case report forms or
electronic data capture.
Unlike some CROs, we enhance traditional services through technology. By using ClinPlus® Data Management (CPDM), a comprehensive 21 CFR Part 11-compliant SAS®-based system, we offer optimal flexibility and effcacy of data management from database design to end of study. For example, we do not have to commit to either paper or EDC; we have the ability to utilize both within CPDM, as well as merge data and provide options for the sites. Instead of the typical database build time and additional time for programming electronic edit checks and listings, CPDM provides the tools to utilize SAS® within the building simultaneously, which significantly reduces the time from CRF design to final database into production with data cleaning tools. Additionally, data is entered into SAS® data sets so that it is instantly accessible for analysis. By managing all of your data processing procedures with one system, you are ensured a smooth progression from entry of the first casebook to a clean and locked database.
At ResearchPoint, our goal is to provide the ideal outsourcing
experience for our customers, from study start-up to final report.
Our continuum model of integrated services helps us consistently
improve the outsourcing experience for our customers and
theirs, the investigators.