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.