FDA issued a request for comment on its recall regulations and their estimated reporting burdens in early August. FDA explicitly invites comments on: ● whether proposed collection of information is necessary for the proper performance of the agency’s functions ● the accuracy of FDA’s estimate of the burden of the proposed collection of information ● ways to enhance the quality, utility, and clarity of the information to be collected, and ● ways to minimize the burden of the collection of information. The comment period is open until October 3.
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