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Live webinar: Making Dissolution Compliance and Qualification Your Friend

See why 21 CFR Part 11 compliance and instrument qualification do not have to be a chore

In this webinar, we’ll focus on two key elements of routine dissolution testing in your GMP laboratory: compliance with 21 CFR Part 11 and apparatus qualification. You’ll learn how to:

•	Control test methodology and documentation.
•	Ensure IQ and OQ qualification of your dissolution apparatus.
•	Assess the advantages and limitations of different means of qualification.
•	Manage significant sources of variability in dissolution testing.

Live webinar

Changing the Perspective: Making Dissolution Compliance and Qualification Your Friend

November 13, 2019
10 a.m. ET / 7 a.m. PT

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