The dissolution test is considered one of the main tools for evaluating solid dosage forms. Being properly executed, it allows an in-depth knowledge of the formulation and assists in making decisions about the feasibility of a bioavailability/bioequivalence relative study.

DEINFAR has a space exclusively dedicated to dissolution studies with modern equipment and installations, experience and trained team and publications in several national and international journals, which attests our expertise in this area.

Projects involving dissolution are related to:

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• Development and validation of methodologies for dissolution testing

• Comparative studies of dissolution profiles.

• Assistance for carrying out dissolution tests with the aim of doing previous selection of formulations for bioequivalence studies.

• Theoretical and practical training.