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2012 ISPE Lessons from 483s

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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 Announcements

Event handouts are now available!

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.
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