Federal (United States) · Regulations
Subpart C — Electronic Prescriptions
21 sections
21 sections
- 21 C.F.R. § 1311.100General.
- 21 C.F.R. § 1311.102Practitioner responsibilities.
- 21 C.F.R. § 1311.105Requirements for obtaining an authentication credential—Individual practitioners.
- 21 C.F.R. § 1311.110Requirements for obtaining an authentication credential—Individual practitioners eligible to use an electronic prescription application of an institutional practitioner.
- 21 C.F.R. § 1311.115Additional requirements for two-factor authentication.
- 21 C.F.R. § 1311.116Additional requirements for biometrics.
- 21 C.F.R. § 1311.120Electronic prescription application requirements.
- 21 C.F.R. § 1311.125Requirements for establishing logical access control—Individual practitioner.
- 21 C.F.R. § 1311.130Requirements for establishing logical access control—Institutional practitioner.
- 21 C.F.R. § 1311.135Requirements for creating a controlled substance prescription.
- 21 C.F.R. § 1311.140Requirements for signing a controlled substance prescription.
- 21 C.F.R. § 1311.145Digitally signing the prescription with the individual practitioner's private key.
- 21 C.F.R. § 1311.150Additional requirements for internal application audits.
- 21 C.F.R. § 1311.170Transmission requirements.
- 21 C.F.R. § 1311.200Pharmacy responsibilities.
- 21 C.F.R. § 1311.205Pharmacy application requirements.
- 21 C.F.R. § 1311.210Archiving the initial record.
- 21 C.F.R. § 1311.215Internal audit trail.
- 21 C.F.R. § 1311.300Application provider requirements—Third-party audits or certifications.
- 21 C.F.R. § 1311.302Additional application provider requirements.
- 21 C.F.R. § 1311.305Recordkeeping.