
Formal Meetings Between the FDA and Sponsors or Applicants of PDUFA Products: Guidance for Industry
December 2017
Click to view Guidance Document
Formal Meetings Between the FDA and Sponsors or Applicants of PDUFA Products: Guidance for Industry
Dec 2017 |
In this Technical Brief:
Product Type(s):
- Drug Development
Topic(s):
- Prescription Drug User Fee Act
Region(s):
- United States
Full Info:
Resource Type:
Citation:
U.S. Department of Health and Human Services, Food and Drug Administration
Authors: Center for Drug Evaluation and Research
Product type(s):
- Contraceptives
- Hormonal
- Injectables
- MPTs
Topic(s):
- MPTs
- Development
- Regulatory
Region(s)
- United States
URL of resource: