HSIRB FAQ's and Newsletters/Memos
- Frequently Asked Questions (June 2004)
- Consenting Process - TIPS (June 29, 2004)
- HSIRB Policy for Data and Safety Monitoring (November 26, 2003, updated July 14, 2004)
- Advertising for Research Subjects (April 5, 2004)
- Consent Process for Human Subjects (December 16, 2003)
- Recruitment of Protocol Subjects under HIPAA(October 14, 2003)
- Impact on Research of Health Insurance Portability and Accountability Act "HIPAA" (March 20, 2003)
- Changes to the Renewal Application Form and the HSIRB Renewal Process (October 4, 2004)
- January 2006: Obtaining Signatures on the informed consent document
- February 2006: How to Report Enrollment Numbers
- March 2006: How to Write a Consent Document That Your Subjects Can Understand
- May 2006: Who MUST be listed as “Study Staff” on the HS-1A form
- July 2006: Writing a “Progress Report” for the Renewal Applications for Continuing Review
- September 2006: “Strong” Passwords: Protecting Electronic Research Data
- February 2007: When and How to Report a Completed Research Study
- June 2007: Advertising and Recruitment Materials
