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The U.S. Nuclear Regulatory Commission is in the process of rescinding or revising guidance and policies posted on this webpage in accordance with Executive Order 14151 Ending Radical and Wasteful Government DEI Programs and Preferencing, and Executive Order 14168 Defending Women From Gender Ideology Extremism and Restoring Biological Truth to the Federal Government. In the interim, any previously issued diversity, equity, inclusion, or gender-related guidance on this webpage should be considered rescinded that is inconsistent with these Executive Orders.

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NRC Form 483 - Registration Certificate - in vitro Testing With Byproduct Material Under General License

Form Number: NRC Form 483
Form Title: Registration Certificate - In Vitro Testing With Byproduct Material Under General License
Current Edition: 09-30-2024
Authority Directive or Regulation: 10 CFR 31.11
Form Status: Approved by OMB: 3150-0038, Expires: 09/30/2027
Special Instructions:

Instructions

  1. Submit this form to:
    Director, Office of Nuclear Materials Safety and Safeguards ATTN: Materials Safety and Tribal Liaison Branch, MS: T-5 B60 U.S. Nuclear Regulatory Commission, Washington, DC 20555-0001.

    Detailed guidance on making electronic submissions can be obtained by visiting the NRC 's Electronic Submittals Application Web site; by e-mail to MSHD Resource; or by writing the Office of the Chief Information Officer, U.S. Nuclear Regulatory Commission, Washington, DC 20555 -0001.

    (At NRC, a registration number will be assigned and a validated copy of NRC Form 483 will be returned.)

  2. In the box above, print or type the name, address (including Zip Code), telephone number, and e-mail address of the registrant physician, clinical laboratory, hospital, or veterinarian in the practice of veterinary medicine for whom or for which this registration form is filed.

Page Last Reviewed/Updated Wednesday, October 02, 2024