FDA Seeks Input: Elimination of Regulations

In January 2017, President Trump issued Executive Order 13771 entitled “Reducing Regulation and Controlling Regulatory Costs” and Executive Order 13777 entitled “Enforcing the Regulatory Reform Agenda.” On September 7, FDA Voice reported “FDA’s plan to engage the public in the agency’s new effort to strengthen and modernize FDA’s regulatory framework.” Shortly thereafter, FDA began opening dockets seeking comment. PDG has extensive experience in drafting Citizen Petitions and comments to various dockets. Click here to request assistance. Among the new dockets are the following:

Review of Existing General Regulatory and Information Collection Requirements of Food and Drug Administration

Review of Existing Center for Drug Evaluation and Research Regulatory and Information Collection Requirements

Review of Existing Center for Biologics Evaluation and Research Regulatory and Information Collection Requirements

Review of Existing Center for Devices and Radiological Health Regulatory and Information Collection Requirements

Review of Existing Center for Veterinary Medicine Regulatory and Information Collection Requirements

Review of Existing Center for Tobacco Products Regulatory and Information Collection Requirements

Click here for the full story from FDA Voice.

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