Oct 2, 2020 10:15 am
ActivityOP8600 Research Ethics Administration
Records Series

11 - Health Sciences Research Ethics Board Files

OPRResearch Ethics Compliance
DescriptionIncludes but is not limited to: written procedures, membership lists, lists of affiliations/occupations of members, correspondence, HSREB agendas, minutes of meetings, annual reports and any other documents that the HSREB may require to fulfill its responsibilities. Not used for the review of research ethics applications; see -30 and -31.
Retention TriggerAY
Total Retention 15 years
Final ActionAR
Disposition Plan
Retention Rationale

Food and Drug Regulations (C.R.C., c. 870) DIVISION 5 Drugs for Clinical Trials Involving Human Subjects - Records - C.05.012(4)

The sponsor shall maintain all records referred to in this Division for a period of 15 years.

Natural Health Products Regulations (SOR/2003-196) PART 4 Clinical Trials Involving Human Subjects - Records - 76(4)

The sponsor shall maintain all records referred to in this Part for a period of 15 years.

PIBNo
Vital Records

This schedule applies to official records in all media. Convenience or duplicate copies of official records are considered transitory and should not be kept longer than necessary, and in no event longer than the official copy.



GLOSSARY

  • AR = Transfer to Archives
  • AY = End of Academic Year
  • CO = Continuous OVerwrite
  • CY = End of Calendar Year
  • D = Destroy / Delete
  • DP = Special Disposition Plan
  • FY = End of Fiscal Year
  • OPR = Office of Primary Responsibility
  • PIB = Personal Information Bank


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