Dissolution testing has emerged as a critical test methodology used throughout the life cycle of solid oral dose drug products. Applications for in vitro dissolution testing include the following:

• Predict and model the in vivo performance (or bioavailability) of the drug product
• Guide formulation development
• Monitor the effects of changes to the production process
• Demonstrate bioequivalence
• Monitor lot-to-lot quality of the drug product
• Serve as a quality control test

Dissolution testing at Parsolex spans all phases of drug development. Parsolex uses dissolution testing during formulation design and selection as an essential tool to……

Download our PDF to learn more about compliant dissolution testing methodologies to support your drug development efforts.

Why Choose Parsolex?

Parsolex offers dissolution testing of solid oral dosage forms with a focus on the client experience. We are committed to fully understand our clients’ requirements and to deliver each project on agreed upon timelines. Parsolex brings in-depth experience with analytical technologies for testing pharmaceuticals and a comprehensive understanding of the latest regulatory guidance. We are committed to the highest level of quality and attention to detail to make sure each dissolution study is successfully executed.

Contact us today to discuss how we can support your Dissolution and Drug Release Testing needs.