Conducting Research in a Hospital

• The Queen’s University Health Sciences and Affiliated Teaching Hospitals Research Ethics Board
  • Submitting a Research Study for the First Time?
  • Renewing a Research Study Already Approved?
  • Amending a Research Study Already Approved?
  • Serious Adverse Events?
  • Sample of a Consent Form
• The KGH/HDH Research Approval Form
• Clinical Trials
  • What is a Clinical Trial?
  • The Different Phases of a Clinical Trial?
  • Source Documentation?
  • Standard Operating Procedures (SOPs)?
  • Adverse Events and Reporting?
  • Sample of Source Documents
• Clinical Trials Registry
  • What is the Clinical Trial Registry?
  • How do I Register a Clinical Trial?
  • How do I Create, Modify or View a Clinical Trial Record on the Registry?
• The Pharmaceutical & Therapeutics Committee
• The Use of Pharmacy Services for Research
• The Animal Care Committee
• The Biohazards Committee
• The Radiation Safety Committee
• Contracts
• Accessing Patient Data for Research
  • KGH/HDH Data Request Form for Pulling Medical Records
  • Confidentiality Agreement for Accessing Information by Non-Hospital Staff
  • Kingston General Hospital’s Basic Rules of Confidentiality
  • Patient Consent for Contact for Research
• Policies and Statements for Conducting Research with Humans
• Research Hospital Policies
• Publication
• Research by Students and Residents
  • Guidelines for Deciding Whether Studies at Kingston General Hospital Require Research Procedures
• Library Services for Researchers and Staff