Postapproval Methods to Capture Safety and Efficacy Data for Cell and Gene Therapy Products; Draft Guidance for Industry; Availability

1 organizations filed 1 public comment on Postapproval Methods to Capture Safety and Efficacy Data for Cell and Gene Therapy Products; Draft Guidance for Industry; Availability, at the Food and Drug Administration. The comment window closed 216d ago.

Abstract

OPEN

Commenters (1)

• Parenteral Drug Associationtrade assoc.

  1 filing · confidence 97%