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• May include any research or technical project undertaken at MURR which does not have an overriding regulatory classification as a radiological material transfer, a reactor-related design or fabrication project, or an FDA or NRC regulated project.
  • Correspondence regarding objectives and methodology of project
  • Resultant papers, publications, posters, presentations, or data packages
  • Final report on project
• These include student work, graduate and undergraduate, as well as MURR staff produced work. Included are theses, supporting projects, experiments, and facility and component design
• Audit Reports
• QA or other internal audits not FDA regulated
• Customer/supplier audits not FDA regulated
• Tracking and trending records

Series Cutoff: Date of Creation

Disposition Action: Transfer to Archives for Evaluation

Notes and Citations:

• Business and Operational Need (7 years) – Service Reports, research and technical project files, GxP Quality Program Audits
• For research and Technical Projects: If required by any regulatory group, retain as part of the project or program it supports. Otherwise, retain a copy for the period of reference and forward originals to any of the campus academic department(s) involved.