Skip to main content

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: GLTS.Resource@nrc.gov or
    Director, Office of Nuclear Materials Safety and Safeguards ATTN: General License Tracking System (GLTS) U.S. Nuclear Regulatory Commission, Washington, DC 20555-0001.

    Signature required mail may be sent to:
    Director, Office of Nuclear Materials Safety and Safeguards 
    ATTN:   General License Tracking System (GLTS), 
    U.S. Nuclear Regulatory Commission, 
    11555 Rockville Pike, Rockville, MD 20852-2738.

    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

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

B.    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 Thursday, September 03, 2026

Page Last Reviewed/Updated Thursday, September 03, 2026