(a) The laboratory must establish and follow written policies and procedures for each of the following, if applicable:
- (1) Patient preparation.
- (2) Specimen collection.
- (3) Specimen labeling, including patient name or unique patient identifier and, when appropriate, specimen source.
- (4) Specimen storage and preservation.
- (5) Conditions for specimen transportation.
- (6) Specimen processing.
- (7) Specimen acceptability and rejection.
- (8) Specimen referral.
- (b) The laboratory must document the date and time it receives a specimen.
- (c) The laboratory must refer a specimen for testing only to a CLIA-certified laboratory or a laboratory meeting equivalent requirements as determined by CMS.
- (d) If the laboratory accepts a referral specimen, written instructions must be available to the laboratory's clients and must include, as appropriate, the information specified in paragraphs (a)(1) through (a)(7) of this section.