Comparative Dissolution Testing
Ensuring compliance and quality for your pharmaceutical products
Reliable Dissolution Testing for Quality Control
Dissolution testing is a cornerstone of the drug development lifecycle, crucial for maintaining quality control and monitoring the final formulation and manufacturing process of dosage forms.
Profarma offers dissolution testing of pharmaceutical drug products according to applicable pharmacopeial monographs or in-house methods, ensuring the highest standards of quality and compliance.
Frequently Asked Questions
What is comparative dissolution testing?
Comparative dissolution testing involves comparing the dissolution profiles of a test product (such as a generic drug) and a reference product (such as a branded drug) to ensure they release their active ingredients at a similar rate and extent under standardized conditions.
What types of products require comparative dissolution testing?
Comparative dissolution testing is commonly required for:
- Generic drugs
- Modified-release formulations
- New formulations of existing drugs
- Products undergoing post-approval changes
How does Profarma conduct comparative dissolution testing?
Profarma conducts comparative dissolution testing using state-of-the-art equipment and standardized methods. We perform tests under various conditions to simulate different physiological environments, ensuring comprehensive comparison and analysis.
How can I get started with Profarma’s comparative dissolution testing services?
To begin, contact Profarma through our website. Our team will discuss your specific needs and provide a tailored proposal for comparative dissolution testing to ensure your product meets all regulatory and quality standards.