Medical Device Submissions: Amending Premarket Regulations that Require Multiple Copies and Specify Paper Copies to be Allowed in Electronic Format; Companion to Direct Final Rule.

2 organizations filed 2 public comments on Medical Device Submissions: Amending Premarket Regulations that Require Multiple Copies and Specify Paper Copies to be Allowed in Electronic Format; Companion to Direct Final Rule., at the Food and Drug Administration. The comment window closed 2785d ago.

Commenters (2)

• Advanced Medical Technology Associationtrade assoc.

  1 filing · confidence 97%
• Medical Imaging & Technology Alliancetrade assoc.

  1 filing · confidence 97%