|Articles|March 15, 2003
- BioPharm International-03-01-2003
- Volume 16
- Issue 3
Inside Washington: The Big Shift
Author(s)Jill Wechsler
Jill Wechsler FDA explains its plan for moving most biologics under the authority of CDER. But a big question remains: What will the change do to approval times?
Advertisement
Articles in this issue
almost 23 years ago
Biotech World: India Blossomsalmost 23 years ago
Outsourcing Outlook: One-Stop Shopsalmost 23 years ago
Qualification of a Chromatographic Column: Why and How to Do Italmost 23 years ago
Guest Editorial: Recruiting Biotech Talentalmost 23 years ago
Survival Strategies: How to Purchase COTS SoftwareNewsletter
Stay at the forefront of biopharmaceutical innovation—subscribe to BioPharm International for expert insights on drug development, manufacturing, compliance, and more.
Advertisement
Advertisement
Advertisement
Trending on BioPharm International
1
How CDMO Alliances Can Provide End-to-End Service that Reduces Drug Development Time and Costs
2
First-in-Human Study Validates Safety of Next-Generation mRNA–LNP Platform
3
Industry Outlook 2026: Key Forces Transforming Drug Pipelines (Part 2)
4
FDA Clears PharmaResearch IND for Nano-Based Cancer Drug PRD-101
5
