21 CFR 1311, Subpart C - Electronic Prescriptions
prev | next
- § 1311.100 — General.
- § 1311.102 — Practitioner responsibilities.
- § 1311.105 — Requirements for obtaining an authentication credential—Individual practitioners.
- § 1311.110 — Requirements for obtaining an authentication credential—Individual practitioners eligible to use an electronic prescription application of an institutional practitioner.
- § 1311.115 — Additional requirements for two-factor authentication.
- § 1311.116 — Additional requirements for biometrics.
- § 1311.120 — Electronic prescription application requirements.
- § 1311.125 — Requirements for establishing logical access control—Individual practitioner.
- § 1311.130 — Requirements for establishing logical access control—Institutional practitioner.
- § 1311.135 — Requirements for creating a controlled substance prescription.
- § 1311.140 — Requirements for signing a controlled substance prescription.
- § 1311.145 — Digitally signing the prescription with the individual practitioner's private key.
- § 1311.150 — Additional requirements for internal application audits.
- § 1311.170 — Transmission requirements.
- § 1311.200 — Pharmacy responsibilities.
- § 1311.205 — Pharmacy application requirements.
- § 1311.210 — Archiving the initial record.
- § 1311.215 — Internal audit trail.
- § 1311.300 — Application provider requirements—Third-party audits or certifications.
- § 1311.302 — Additional application provider requirements.
- § 1311.305 — Recordkeeping.
Title 21 published on 2012-04-01
no entries appear in the Federal Register after this date.
This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.
This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].
It is not guaranteed to be accurate or up-to-date, though we do refresh the database weekly. More limitations on accuracy are described at the GPO site.
