Collaboration Corner :: Research Compliance Newsletter
Collaboration Corner Vol 3 No 7(2)
[Confidentiality/Non-Disclosure and Material Transfer Agreements]
Collaboration Corner Vol 3 No 7(1)
[Confidentiality/Non-Disclosure and Material Transfer Agreements]
Collaboration Corner Vol 3 No 6(2)
[Confidentiality/Non-Disclosure and Material Transfer Agreements]
Collaboration Corner Vol 3 No 6(1)
[Confidentiality/Non-Disclosure and Material Transfer Agreements]
Collaboration Corner Vol 3 No 5(2)
[Confidentiality/Non-Disclosure and Material Transfer Agreements]
Collaboration Corner Vol 3 No 5(1)
[Confidentiality/Non-Disclosure and Material Transfer Agreements]
Collaboration Corner Vol 3 No 4
[Confidentiality/Non-Disclosure and Material Transfer Agreements]
Collaboration Corner Vol 3 No 3
[Confidentiality/Non-Disclosure and Material Transfer Agreements]
Collaboration Corner Vol 3 No 1
[Helpful Tips; Common Non-Compliance Finding; Education Program: New Topic]
Collaboration Corner Vol 2 No 12
[Non-Human Subject Research; Protocol Version Dates; Clinical Trial Registration]
Collaboration Corner Vol 2 No 11
[Assent; Inclusion of children in research]
Collaboration Corner Vol 2 No 10
[Obtaining Gift Cards: CASE & UHCMC; Partial Waivers of Consent and HIPAA Authorization]
Collaboration Corner Vol 2 No 9
[Informed Consent Template; Responsible Conduct of Research Education Seminars and Workshops]
Collaboration Corner Vol 2 No 8
[New Guidelines: Enrollment of Subjects with Decisional Impairment in Research]
Collaboration Corner Vol 2 No 7
[Exempt Research; HIPAA Authorization Reminder; The Office of Technology Management]
Collaboration Corner Vol 2 No 6
[IRB Rosters available on-line; Updates to IRB Policies, Procedures, Forms and Templates; Policy Revision: Closure versus Termination]
Collaboration Corner Vol 2 No 5
[Revisions to the Adverse Event Reporting Policy]
Collaboration Corner Vol 2 No 4
[Pregnant Women in Research]
Collaboration Corner Vol 2 No 3
[Common Non-Compliance Findings, Part I: Failure to Report Adverse Events and Other Reportable Events; and NEW: Genetic Research Ethics Consultation Service / Rapid Ethics Action Consult Team]
Collaboration Corner Vol 2 No 2
[Inclusion of Illiterate, non-English speaking subjects, and pregnant women and fetuses in research studies; NEW: HIPAA Authorization Template Language]
Collaboration Corner Vol 2 No 1
[Prompt Reporting of Protocol Amendments; Requirements for Continuing Review Submissions]
Past Research Compliance Newsletters
[An Introduction: Research Collaboration Corner; What is the UHC Office of Research Compliance; Why am I being contacted by the UHC ORC? Research Compliance Monitoring Program; Helpful Tips: Investigator Drug Services]
[Research Compliance Monitoring Program…What to expect; Helpful Tips: Reporting Adverse Events for Related Studies]
[Revisions to the UHC IRB Policies and Procedures Manual Helpful Tips; The General Clinical Research Center; Update your contact information]
[Regulatory Binder: Definition and Content; Helpful Tip: Human Tissues and Histology Services]
[Documentation of the Informed Consent Process; New UHC IRB Procedure: Advertisements to Receive an Approval Stamp; Helpful Tip : When to File an Informed Consent Document in a Patient’s Medical Records]
[Obtaining Laboratory Reference Ranges for Regulatory Binders; Update: Clinical Trials Brochure Available Online; Revisions to the UHC IRB Policies and Procedures; Protocol Summary at Continuing Review; Certification Pursuit Program (CPP)]
[Informed Consent Observations; Monitoring: Grants and Contracts; Helpful Tip : How to “Track Changes” in Research Documents]
[Recruitment Material; Privacy versus Confidentiality; Helpful Tip: Who can be a Principal Investigator]
[2007 Monitoring Schedule; Laboratory Reference Ranges: Update for Regulatory Binder; Top 10 Monitoring Findings: 2006]