Thursday 3rd July, 2014
9:00am to 5:00pm
Dissolution testing poses a major challenge to the pharmaceutical, biotech and generics industries both in terms of method development and regulatory compliance.
On this course delegates will gain a thorough understanding of setting and establishing specifications for optimum dissolution testing.
Clarify global regulatory requirements
Assess new scientific developments and trends
Design optimum method development strategies
Identify the factors affecting dissolution
Drive product performance and quality control
Study design considerations for IVIVC Studies
Book before the 5th June 2014: £1,395.00 + (VAT 19.00) = £1,660.05
Book after the 5th June 2014: £1,495.00 + (VAT 19.00) = £1,779.05
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