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- 20 CFR 1010.330 · What are the responsibilities of recipients to collect and maintain data on covered and non-covered persons?
- 20 CFR 1011.000 · What is the HIRE Vets Medallion Program?
- 20 CFR 1011.005 · What definitions apply to this part?
- 20 CFR 1011.010 · Who is eligible to apply for a HIRE Vets Medallion Award?
- 20 CFR 1011.015 · What are the different types of the HIRE Vets Medallion Awards?
- 20 CFR 1011.100 · What are the criteria for the large employer HIRE Vets Medallion Award?
- 20 CFR 1011.105 · What are the criteria for the medium employer HIRE Vets Medallion Award?
- 20 CFR 1011.110 · What are the criteria for the small employer HIRE Vets Medallion Award?
- 20 CFR 1011.115 · Is there an exemption for certain large employers from the dedicated human resources professional criterion for the large employer platinum HIRE Vets Medallion Award?
- 20 CFR 1011.120 · Under what circumstances will VETS find an employer ineligible to receive a HIRE Vets Medallion Award for a violation of labor law?
- 20 CFR 1011.200 · How will VETS administer the HIRE Vets Medallion Award process?
- 20 CFR 1011.205 · What is the timing of the HIRE Vets Medallion Award process?
- 20 CFR 1011.210 · How often can an employer receive the HIRE Vets Medallion Award?
- 20 CFR 1011.215 · How will the employer complete the application for the HIRE Vets Medallion Award?
- 20 CFR 1011.220 · How will VETS verify a HIRE Vets Medallion Award application?
- 20 CFR 1011.225 · Under what circumstances will VETS conduct further review of an application?
- 20 CFR 1011.230 · Under what circumstances can VETS deny or revoke an award?
- 20 CFR 1011.300 · What are the application fees for the HIRE Vets Medallion Award?
- 20 CFR 1011.305 · May VETS set a limit on how many applications will be accepted in a year?
- 20 CFR 1011.400 · What does a successful applicant receive?
- 20 CFR 1011.405 · What are the restrictions on display and use of the HIRE Vets Medallion Award?
- 20 CFR 1011.500 · What is the process to request reconsideration of a denial or revocation?
- 20 CFR 1011.600 · What are the record retention requirements for the HIRE Vets Medallion Award?
- 21 CFR 1.1 · General.
- 21 CFR 1.3 · Definitions.
- 21 CFR 1.4 · Authority citations.
- 21 CFR 1.20 · Presence of mandatory label information.
- 21 CFR 1.21 · Failure to reveal material facts.
- 21 CFR 1.23 · Procedures for requesting variations and exemptions from required label statements.
- 21 CFR 1.24 · Exemptions from required label statements.
- 21 CFR 1.70 · Scope.
- 21 CFR 1.71 · Definitions.
- 21 CFR 1.72 · Data elements that must be submitted in ACE for articles regulated by FDA.
- 21 CFR 1.73 · Food.
- 21 CFR 1.74 · Human drugs.
- 21 CFR 1.75 · Animal drugs and veterinary devices.
- 21 CFR 1.76 · Medical devices.
- 21 CFR 1.77 · Radiation-emitting electronic products.
- 21 CFR 1.78 · Biological products, HCT/Ps, and related drugs and medical devices.
- 21 CFR 1.79 · Tobacco products.
- 21 CFR 1.80 · Cosmetics.
- 21 CFR 1.81 · Rejection of entry filing.
- 21 CFR 1.83 · Definitions.
- 21 CFR 1.90 · Notice of sampling.
- 21 CFR 1.91 · Payment for samples.
- 21 CFR 1.94 · Hearing on refusal of admission or destruction.
- 21 CFR 1.95 · Application for authorization to relabel and recondition.
- 21 CFR 1.96 · Granting of authorization to relabel and recondition.
- 21 CFR 1.97 · Bonds.
- 21 CFR 1.99 · Costs chargeable in connection with relabeling and reconditioning inadmissible imports.
- 21 CFR 1.101 · Notification and recordkeeping.
- 21 CFR 1.225 · Who must register under this subpart?
- 21 CFR 1.226 · Who does not have to register under this subpart?
- 21 CFR 1.227 · What definitions apply to this subpart?
- 21 CFR 1.230 · When must you register or renew your registration?
- 21 CFR 1.231 · How and where do you register or renew your registration?
- 21 CFR 1.232 · What information is required in the registration?
- 21 CFR 1.233 · Are there optional items included in the registration form?
- 21 CFR 1.234 · How and when do you update your facility's registration information?
- 21 CFR 1.235 · How and when do you cancel your facility's registration information?
- 21 CFR 1.240 · What other registration requirements apply?
- 21 CFR 1.241 · What are the consequences of failing to register, update, renew, or cancel your registration?
- 21 CFR 1.242 · What does assignment of a registration number mean?
- 21 CFR 1.243 · Is food registration information available to the public?
- 21 CFR 1.245 · Waiver request.
- 21 CFR 1.276 · What definitions apply to this subpart?
- 21 CFR 1.277 · What is the scope of this subpart?
- 21 CFR 1.278 · Who is authorized to submit prior notice?
- 21 CFR 1.279 · When must prior notice be submitted to FDA?
- 21 CFR 1.280 · How must you submit prior notice?
- 21 CFR 1.281 · What information must be in a prior notice?
- 21 CFR 1.282 · What must you do if information changes after you have received confirmation of a prior notice from FDA?
- 21 CFR 1.283 · What happens to food that is imported or offered for import without adequate prior notice?
- 21 CFR 1.284 · What are the other consequences of failing to submit adequate prior notice or otherwise failing to comply with this subpart?
- 21 CFR 1.285 · What happens to food that is imported or offered for import from unregistered facilities that are required to register under subpart H of this part?
- 21 CFR 1.326 · Who is subject to this subpart?
- 21 CFR 1.327 · Who is excluded from all or part of the regulations in this subpart?
- 21 CFR 1.328 · What definitions apply to this subpart?
- 21 CFR 1.329 · Do other statutory provisions and regulations apply?
- 21 CFR 1.330 · Can existing records satisfy the requirements of this subpart?
- 21 CFR 1.337 · What information must nontransporters establish and maintain to identify the nontransporter and transporter immediate previous sources of food?
- 21 CFR 1.345 · What information must nontransporters establish and maintain to identify the nontransporter and transporter immediate subsequent recipients of food?
- 21 CFR 1.352 · What information must transporters establish and maintain?
- 21 CFR 1.360 · What are the record retention requirements?
- 21 CFR 1.361 · What are the record availability requirements?
- 21 CFR 1.362 · What records are excluded from this subpart?
- 21 CFR 1.363 · What are the consequences of failing to establish or maintain records or make them available to FDA as required by this subpart?
- 21 CFR 1.368 · What are the compliance dates for this subpart?
- 21 CFR 1.377 · What definitions apply to this subpart?
- 21 CFR 1.378 · What criteria does FDA use to order a detention?
- 21 CFR 1.379 · How long may FDA detain an article of food?
- 21 CFR 1.380 · Where and under what conditions must the detained article of food be held?
- 21 CFR 1.381 · May a detained article of food be delivered to another entity or transferred to another location?
- 21 CFR 1.382 · What labeling or marking requirements apply to a detained article of food?
- 21 CFR 1.383 · What expedited procedures apply when FDA initiates a seizure action against a detained perishable food?
- 21 CFR 1.384 · When does a detention order terminate?
- 21 CFR 1.391 · Who approves a detention order?
- 21 CFR 1.392 · Who receives a copy of the detention order?
- 21 CFR 1.393 · What information must FDA include in the detention order?
- 21 CFR 1.401 · Who is entitled to appeal?