Diagnostic and Clinical Division Correspondence, Forms, SOPs
Record description
Compliance monitoring data should be made legally defensible by keeping thorough and accurate records. The Quality Assurance (QA) plan and/or Standard Operating Procedures (SOPs) need to describe the policies and procedures used by the facility for record integrity, retention, and storage (EPA Order 5360.1). Be able to reconstruct all testing with data.
UI retention guidelines
5 years after a procedure has been discontinued (per the Clinical Laboratories Improvement Amendment)
Official files maintained by
State Hygienic Laboratory
Record category
State Hygienic Laboratory