The U.S. FDA wants your input — by December 4 this year

Do you have views on how the U.S. Food and Drug Administration (FDA) should be seeking and obtaining the views of patients during the development process for drugs and medical devices, and on ways to consider patients’ perspectives during regulatory discussions about the evaluation and approval of such products?

If you do, now’s your chance!

The FDA is asking for all stakeholders to provide input and to contribute to this discussion. You can do it as an individual or you can do it through a specific organization you may belong to or however else you may want to. However, you do need to do it by December 4, and you do need to do it using the FDA’s formal document management system, as described on pages 65410 and 65411 of Vol. 69 of The Federal Register.

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