2012 ISPE Lessons from 483s
Discover how to combine the best in science and engineering to deliver low cost operations and high quality products.
This conference will review recent regulatory citations (FDA-483s) and provide guidance on how the citations could be avoided.
Tracks: Biotech Oral Solid Dosage Process Validation
Event handouts are now
Don't miss a presentation by the FDA's Grace McNally, Process Validation Subject Matter Expert
Track Agendas Now Available
Special Thanks to the 483s Processing Conference Program Committee.