Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products Marketed Without an Approved Application

1 organizations filed 1 public comment on Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products Marketed Without an Approved Application, at the Food and Drug Administration. The comment window closed 2843d ago.

Abstract

Agency Information Collection Activities; Announcement of Office of Management and Budget Approval

Commenters (1)

• Consumer Healthcare Products Associationtrade assoc.

  1 filing · confidence 97%