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- Priority Review of Drug Submissions
- Notice of compliance with conditions
- Interim Order Respecting the Importation, Sale and Advertising of Drugs for Use in Relation to COVID-19.

- Article 170
- Equivalence Agreement
- Recognition of MAs from Reference Authorities

- FDA Breakthrough Therapy
- FDA Accelerated Approval
- FDA CPP for Unapproved Products
- FDA Fast Track
- FDA Orphan Designation
- FDA Priority Review
- FDA Real Time Oncology Review-RTOR
- FDA Regenerative Medicine Advanced Therapy Designation
- Limited Population Pathway for Antibacterial and Antifungal Drugs
- Split Real-Time Application Review (STAR) Program
- Coronavirus Treatment Acceleration Program (CTAP)
- Accelerating Rare disease Cures (ARC) Program
- Innovative Science and Technology Approaches for New Drugs (ISTAND) Pilot Program
- Emergency Use Authorization (EUA)
- Emergency Use Authorization for Vaccines to Prevent COVID-19
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