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
Compita Consulting IRB Services
Expert Guidance for Human Research Protection
Contact us
Office: 785-410-8003
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