To request an Application to Conduct Research, please contact the IRB office:
Telephone: (805) 696-7916 FAX: (805) 681-6495 E-mail: Leilani Price or Tamara Norton
POLICY
TITLE (HTML document)
WORD document
8012.01
Non-Affiliated Investigator Agreement
8012.02
Adverse Event Reporting
Offsite Adverse Event Report form (Word document only)
Onsite Adverse Event Report form (Word document only)
8012.03
Billing for IRB Review of Research
8012.04
Research Subject Recruitment and Advertisement
8012.05
Investigator Responsibilities
8012.06
IRB Review of Research
Attachment A: Categories of Research for Expedited Review (Word document only)
Attachment B: Categories of Research Exempt from Review (Word document only)
8012.07
Guideline for Surrogate Consenting
8012.08
Emergency Use of a Test Article
8012.09
Institutional Review Board Membership
8012.10
IRB Records and Reporting Guidelines
8012.11
Guidelines for Securing and Documenting Patient Authorization
8012.12
Specimen Collection and/or Tissue Banking
8012.13
Informed Consent Guidelines
8012.14
Conflict of Interest
8012.15
Reporting Guidelines for Off-Site Research and Research Approved by Other IRBs
8012.16
CHS IRB Approval of Research Conducted Outside Cottage Health System
8012.17
IRB Education, Compliance, and Audit Activities
8012.18
8012.19
Guidelines for the Compassionate Use of Investigational Agents
8012.20
Children's Assent Guidelines
8012.22
Inclusion of Women and Minorities in Research
8012.23
Medical Device Guidelines
8012.25
NCI CIRB Cooperative Research
8012.26
Reporting Guidelines for CCSB for TORI Research Network
