The U.S. Nuclear Regulatory Commission (NRC) has requested a renewal of an information collection with the Office of Management and Budget (OMB) for NRC Form 483, titled "Registration Certificate—In Vitro Testing with Byproduct Material Under General License." This renewal affects physicians, veterinarians, clinical laboratories, and hospitals that need a general license to use certain byproduct materials for in vitro testing. The NRC is accepting comments on this proposal until February 11, 2021 and encourages electronic submissions through the Federal Rulemaking website. The information collected helps ensure that license holders are authorized to handle specific materials, contributing to safety and regulatory compliance.
Simple Explanation
The NRC wants to keep collecting forms from doctors and labs who use special materials for tests, to make sure they can use them safely. They are asking for ideas on this plan until February 11, 2021.