We offer a complimentary 30 minute session to assess your needs! (785)410-8003, irb@COMPITACONSULTING.coM book your appoinTMENT TODAY!

Services & Pricing

We provide expert review, monitoring and approval of research, dissertation development and consulting services, auditing and monitoring of research and education and training for researchers.

Institutional Review Board

  • Non-human subject determinations

  • Non-research determination

  • Exemption determinations

  • Expedited review

  • Informed consent

  • General/generic recruitment (or advertising)

  • Continuing review

  • Amendments/modifications

  • Deviations/unanticipated problems

  • Closeout

    We contract with an external IRB to review clinical trials

Education Programs

  • Clinical Research Coordinator 101 Course

  • Institutional Review Board 101 Course

  • Institutional Review Board Processes 101

  • Community Board Member 101

  • Exempt Review Course 101

  • Expedited Review Course 101

  • Full Board Review Course 101

Contact for group session and pricing information

Auditing & Monitoring

  • 3 groups of services:

  • Group 1 offers GCP auditing

  • Group 2 ensures all regulatory requirements are met

  • Group 3 assesses whether clinical components are met

Monitoring

  • Develop a monitoring plan

  • Monitoring strategy

  • Monitoring methods

  • Monitoring of critical data and processes

  • Routine monitoring

  • Training

Consulting & Dissertation Help

  • Consult with a coach (all hold doctorates)

  • Protocol development

  • IRB application completion

  • Informed consent writing

  • Questionnaire development

  • Setting up an IRB or ethics committee

  • IRB process evaluation and enhancement

  • IRB compliance evaluations

  • Policies, procedures, forms, and checklists

  • Training and education

  • IRB review consultations

  • Temporary IRB members

  • Temporary IRB staff