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- 21 CFR 1311.20 · Coordinators for CSOS digital certificate holders.
- 21 CFR 1311.25 · Requirements for obtaining a CSOS digital certificate.
- 21 CFR 1311.30 · Requirements for storing and using a private key for digitally signing orders.
- 21 CFR 1311.35 · Number of CSOS digital certificates needed.
- 21 CFR 1311.40 · Renewal of CSOS digital certificates.
- 21 CFR 1311.45 · Requirements for registrants that allow powers of attorney to obtain CSOS digital certificates under their DEA registration.
- 21 CFR 1311.50 · Requirements for recipients of digitally signed orders.
- 21 CFR 1311.55 · Requirements for systems used to process digitally signed orders.
- 21 CFR 1311.60 · Recordkeeping.
- 21 CFR 1311.100 · General.
- 21 CFR 1311.102 · Practitioner responsibilities.
- 21 CFR 1311.105 · Requirements for obtaining an authentication credential—Individual practitioners.
- 21 CFR 1311.110 · Requirements for obtaining an authentication credential—Individual practitioners eligible to use an electronic prescription application of an institutional practitioner.
- 21 CFR 1311.115 · Additional requirements for two-factor authentication.
- 21 CFR 1311.116 · Additional requirements for biometrics.
- 21 CFR 1311.120 · Electronic prescription application requirements.
- 21 CFR 1311.125 · Requirements for establishing logical access control—Individual practitioner.
- 21 CFR 1311.130 · Requirements for establishing logical access control—Institutional practitioner.
- 21 CFR 1311.135 · Requirements for creating a controlled substance prescription.
- 21 CFR 1311.140 · Requirements for signing a controlled substance prescription.
- 21 CFR 1311.145 · Digitally signing the prescription with the individual practitioner's private key.
- 21 CFR 1311.150 · Additional requirements for internal application audits.
- 21 CFR 1311.170 · Transmission requirements.
- 21 CFR 1311.200 · Pharmacy responsibilities.
- 21 CFR 1311.205 · Pharmacy application requirements.
- 21 CFR 1311.210 · Archiving the initial record.
- 21 CFR 1311.215 · Internal audit trail.
- 21 CFR 1311.300 · Application provider requirements—Third-party audits or certifications.
- 21 CFR 1311.302 · Additional application provider requirements.
- 21 CFR 1311.305 · Recordkeeping.
- 21 CFR 1312.01 · Scope of part 1312.
- 21 CFR 1312.02 · Definitions.
- 21 CFR 1312.03 · Forms applicable to this part.
- 21 CFR 1312.11 · Requirement of authorization to import.
- 21 CFR 1312.12 · Application for import permit; return information.
- 21 CFR 1312.13 · Issuance of import permit.
- 21 CFR 1312.14 · Distribution of import permits.
- 21 CFR 1312.15 · Shipments in greater or less amount than authorized.
- 21 CFR 1312.16 · Amendment, cancellation, expiration of import permit.
- 21 CFR 1312.17 · Special report from importers.
- 21 CFR 1312.18 · Import declaration.
- 21 CFR 1312.19 · Distribution of import declaration.
- 21 CFR 1312.21 · Requirement of authorization to export.
- 21 CFR 1312.22 · Application for export or reexport permit; return information.
- 21 CFR 1312.23 · Issuance of export permit.
- 21 CFR 1312.24 · Distribution of export permit.
- 21 CFR 1312.25 · Amendment, cancellation, expiration of export permit.
- 21 CFR 1312.26 · Records required of exporter.
- 21 CFR 1312.27 · Export/reexport declaration.
- 21 CFR 1312.28 · Distribution of export declaration.
- 21 CFR 1312.29 · Domestic release prohibited.
- 21 CFR 1312.30 · Schedule III, IV, and V non-narcotic controlled substances requiring an import and export permit.
- 21 CFR 1312.31 · Schedule I: Application for prior written approval.
- 21 CFR 1312.32 · Schedules II, III, IV: Advance notice.
- 21 CFR 1312.41 · Hearings generally.
- 21 CFR 1312.42 · Purpose of hearing.
- 21 CFR 1312.43 · Waiver or modification of rules.
- 21 CFR 1312.44 · Request for hearing or appearance; waiver.
- 21 CFR 1312.45 · Burden of proof.
- 21 CFR 1312.46 · Time and place of hearing.
- 21 CFR 1312.47 · Final order.
- 21 CFR 1313.01 · Scope.
- 21 CFR 1313.02 · Definitions.
- 21 CFR 1313.03 · Forms applicable to this part.
- 21 CFR 1313.05 · Requirements for an established business relationship.
- 21 CFR 1313.08 · Requirements for establishing a record as an importer.
- 21 CFR 1313.12 · Notification prior to import.
- 21 CFR 1313.13 · Requirements of import declaration.
- 21 CFR 1313.14 · Disposition of import declaration.
- 21 CFR 1313.15 · Qualification of regular importers.
- 21 CFR 1313.16 · Updated notice for change in circumstances.
- 21 CFR 1313.17 · Return declaration for imports.
- 21 CFR 1313.21 · Notification prior to export.
- 21 CFR 1313.22 · Export declaration.
- 21 CFR 1313.23 · Disposition of export declaration.
- 21 CFR 1313.24 · Waiver of 15-day advance notice for chemical exporters.
- 21 CFR 1313.25 · Foreign import restrictions.
- 21 CFR 1313.26 · Updated notice for change in circumstances.
- 21 CFR 1313.27 · Return declaration for exports.
- 21 CFR 1313.31 · Advance notice of importation for transshipment or transfer.
- 21 CFR 1313.32 · Notification of international transactions.
- 21 CFR 1313.33 · Contents of an international transaction declaration.
- 21 CFR 1313.34 · Disposition of the international transaction declaration.
- 21 CFR 1313.35 · Return declaration or amendment to Form 486 for international transactions.
- 21 CFR 1313.41 · Suspension of shipments.
- 21 CFR 1313.42 · Prohibition of shipments from certain foreign sources.
- 21 CFR 1313.51 · Hearings generally.
- 21 CFR 1313.52 · Purpose of hearing.
- 21 CFR 1313.53 · Waiver of modification of rules.
- 21 CFR 1313.54 · Request for hearing.
- 21 CFR 1313.55 · Burden of proof.
- 21 CFR 1313.56 · Time and place of hearing.
- 21 CFR 1313.57 · Final order.
- 21 CFR 1314.01 · Scope.
- 21 CFR 1314.02 · Applicability.
- 21 CFR 1314.03 · Definitions.
- 21 CFR 1314.05 · Requirements regarding packaging of nonliquid forms.
- 21 CFR 1314.10 · Effect on State laws.
- 21 CFR 1314.15 · Loss reporting.
- 21 CFR 1314.20 · Restrictions on sales quantity.