16 CFR Part 1702
19 sections.
- § 1702.1§ 1702.1 Purpose and policy.
- § 1702.2§ 1702.2 Procedural requirements and recommendations.
- § 1702.3§ 1702.3 Substantive requirements.
- § 1702.4§ 1702.4 Petitions with insufficient or incomplete information.
- § 1702.5§ 1702.5 Failure to supply adverse information.
- § 1702.6§ 1702.6 Trade secrets and other confidential information.
- § 1702.7§ 1702.7 Justification for the exemption.
- § 1702.8§ 1702.8 Human experience data.
- § 1702.9§ 1702.9 Relevant experimental data.
- § 1702.10§ 1702.10 Human experimental data involving the testing of human subjects.
- § 1702.11§ 1702.11 Product specifications.
- § 1702.12§ 1702.12 Packaging specifications.
- § 1702.13§ 1702.13 Labeling and packaging samples.
- § 1702.14§ 1702.14 Marketing history.
- § 1702.15§ 1702.15 Petitions alleging the incompatibility of child resistant packaging with the particular substance petitioned for exemption.
- § 1702.16§ 1702.16 Petitions requesting an exemption for a drug or a new drug.
- § 1702.17§ 1702.17 Granting petitions.
- § 1702.18§ 1702.18 Denying petitions.
- § 1702.19§ 1702.19 Effect of filing petition.
This is legal information, not legal advice. Laws vary by jurisdiction and change frequently. Always verify current law with official sources and consult a licensed attorney in your jurisdiction for advice on your specific situation.