CONSULTING and TRAINING SERVICES
Our consulting services allows Sponsors, Investigators and Research
Professionals access to a clinical research management team that will simplify
processes, reduce error an reduce cost.
- Independent Site Monitoring and Quality Assurance Program
ReSolve will independently monitor the site and attend Pre-Study Selection
Visits (PSSV), Site Initiation Visits (SIV), Interim Monitoring Visit and
Site Closeout Visits on behalf of the Investigator or the Sponsor. Follow up
reports are sent to the Site and Sponsor to ensure queries are resolved and
information is consistent.
- Surveys
RRS, Inc. assists companies
and organizations understand the needs of their clients/patients, strategic
partners, and stakeholders through the use of qualitative and
quantitative research methods, including:
- in-depth interviews
- mail, email, and web-based surveys
- telephone surveys
- focus groups
- Protocol Development and CRF Design
- Outsourcing Management
ReSolve will maintain and execute oversight and management of contractors
including CRO's, central laboratories and independent consultants.
- Timeline Tracking
ReSolve will identify and assist clients in establishing and maintaining
study milestones and deadlines throughout the conduct of the clinical trial.
- Training
ReSolve training programs are available for Clinical Research Coordinators
and Investigators. These 1-2 day programs describe all aspects of the
clinical trial and review the roles and responsibilities of all members of
the research team. Contact
us online for course availability and pricing information.
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