Dissolution Testing in Pharmaceutical Analysis

Venue: Holiday Inn Miami Airport

Location: Miami, Florida, United States

Event Date/Time: May 25, 2010 End Date/Time: May 26, 2010
Registration Date: May 26, 2010
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Description

A TWO-DAY COMPREHENSIVE and INTERACTIVE CONFERENCE, with CASE STUDIES, WORKSHOP and EXHIBITION addressing:
Regulatory Requirements for Dissolution Testing
Change in Criteria for USP Dissolution Performance Verification Test
Role of Dissolution Testing in QbD
The Role of Dissolution Testing in Support of Drug Development
Critical Factors for Consideration During Dissolution Method Development
Early Phase Dissolution Development and Specification Setting
Validating Analytical Methods Based on Current ICH Guidance and USP/Industry Standards
The Value of In Vitro Dissolution in Drug Development
Dissolution Challenges: An Industrial perspective
Dissolution Testing and Qualification from a Pharmacopeial Perspective
Current Challenges: Method Transfer and GMP
Dissolution of BCS (Biopharmaceutics Classification System) Class 2, 4 and Novel Dosage Forms
Dissolution and Global Biowaivers
Dissolution, Absorption and IVIVC - The Development of Bio-relevant Dissolution Methods
Current Challenges: Dissolution Equipment –Sources of Error and Performance Verification

Venue

1111 South Royal Poinciana Blvd Miami Springs, FL 33166
Miami
Florida
United States
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