yourstate.us
42 CFR 485.60

§ 485.60 Condition of participation: Clinical records.

United States · 42 CFR — Public Health · Status: effective

Get this as JSONEmbed this
Cite this
Citation
42 CFR 485.60, § 485.60 Condition of participation: Clinical records, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/207342
Permanent ID
ys:prov:207342@1
SHA-256
c64a38e07c1b818301054a6357dc765ab77dd0a90175e1c16ff423a5d71349af

The hash is SHA-256 of this version's text, with every run of whitespace collapsed to a single space and the ends trimmed. The ID always leads back here, and checking it says whether the text you cited is still the current version.

Full text

The facility must maintain clinical records on all patients in accordance with accepted professional standards and practice. The clinical records must be completely, promptly, and accurately documented, readily accessible, and systematically organized to facilitate retrieval and compilation of information. (a) Standard: Content. Each clinical record must contain sufficient information to identify the patient clearly and to justify the diagnosis and treatment. Entries in the clinical record must be made as frequently as is necessary to insure effective treatment and must be signed by personnel providing services. All entries made by assistant level personnel must be countersigned by the corresponding professional. Documentation on each patient must be consolidated into one clinical record that must contain— (1) The initial assessment and subsequent reassessments of the patient's needs; (2) Current plan of treatment; (3) Identification data and consent or authorization forms; (4) Pertinent medical history, past and present; (5) A report of pertinent physical examinations if any; (6) Progress notes or other documentation that reflect patient reaction to treatment, tests, or injury, or the need to change the established plan of treatment; and (7) Upon discharge, a discharge summary including patient status relative to goal achievement, prognosis, and future treatment considerations. (b) Standard: Protection of clinical record information. The facility must safeguard clinical record information against loss, destruction, or unauthorized use. The facility must have procedures that govern the use and removal of records and the conditions for release of information. The facility must obtain the patient's written consent before releasing information not required to be released by law. (c) Standard: Retention and preservation. The facility must retain clinical record information for 5 years after patient discharge and must make provision for the maintenance of such records in the event that it is no longer able to treat patients.

Legislative history

This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.