Training

Salus IRB requires that investigators and key research team members be adequately trained to meet the requirements of the federal regulations and expectations of the board. Investigators and their research team must have a working knowledge of Good Clinical Practices (GCPs) in conducting clinical trials in human research participants.

Salus IRB provides access to training resources to ensure that investigators are prepared to fulfill their responsibilities. Such education and training may include web-based tutorials and/or verification that appropriate training was obtained prior to initiation of research. Salus may also consider previous research experience, as evidenced by the investigator’s CV, in lieu of training.

Salus IRB’s affiliation with the Collaborative Institutional Training Initiative (CITI) allows us to offer our investigators and research team web-based training modules covering GCPs at no cost to you.

Should you choose to utilize this method of training, please follow the steps below:

  1. Register on the site.
  2. Select “Salus IRB” from the dropdown menu under “Subscriber Organizations.”
  3. Select the “Basic Course” and the “GCP Course.”

CITI will notify Salus upon your completion of the modules. CME/CEU credit documentation for this training is available through the CITI website.

Additional Educational and Training Resources

  • OHRP Resources
  • Pharmaceutical Education & Research Institute (PERI)
  • Association of Clinical Research Professionals (ACRP)
  • Drug Information Association (DIA)
Salus IRB
  • About Us
    • Our Boards
    • Your Salus Team
    • Mission and Values
    • Compliance Statement
    • Affiliations
    • News
    • Submission Forms >>
    • Review & Response Times >>
    • Request IRB Roster >>
  • Services
    • Single Site Research/Local Review
    • Multi-Site Research/Central IRB Services
    • Institutional Outsourcing
    • Global/International Review
    • Accelerated Phase I
    • Phase I Oncology
    • Investigator-Initiated/Sponsored Research
    • Minimal Risk Research
    • IRB Exempt Determinations
    • Other Services
    • Getting Started >>
    • Submission Forms >>
    • Contact Us >>
  • Why Salus
    • Getting Started >>
    • Submission Forms >>
    • Review & Response Times >>
  • Getting Started
    • Submission Forms
    • Template Study Documents
    • Review & Response Times
    • Resources
    • Training
    • Contact Us >>
    • Client Feedback Survey >>
  • Sponsors/CROs
    • Reporting Responsibilities
    • Resources
    • Training
    • Getting Started >>
    • Submission Forms >>
    • Review & Response Times >>
  • Investigators
    • Reporting Responsibilities
    • Resources
    • Training
    • Getting Started >>
    • Submission Forms >>
    • Review & Response Times >>
  • Research Participants
    • Participant Inquiries
    • Frequently Asked Questions
    • Resources
  • Resources
    • Thought Leadership
    • For-profit IRBs are on the rise—but at whose expense?
  • Contact Us
    • Client Feedback Survey
    • Salus IRB Team Member Recognition
855.300.0815 SafeSync GlobeSync

© 2022 Salus IRB All Rights Reserved.   •   Salus IRB Privacy Policy   •   Your California Privacy Rights  

Association for the Accredidation of Human Research Protection Programs, Inc.