Monday, August 18, 2008

A Compliance Perspective on Dissolution Method Validation for Immediate-Release Solid Oral Dosage Fo

As the pace of product development accelerates, the approach to dissolution-method development must advance beyond a manual method and an assay. A natural progression of the method-development process must include the transfer of the manual method onto automated instrumentation.

Author(s):
David Fortunato
Journal:
Pharmaceutical Technology, Sep 2, 2006

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Pharmaceutical Validation Documentation Requirements

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