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 are the key applications of dissolution testing?
Dissolution testing is used for:
- Formulation development and optimization
- Quality control of finished products
- Comparative studies for generic drug approval
- Stability testing to assess product shelf life
- Evaluating the impact of manufacturing changes
Can Profarma develop custom dissolution methods?
Yes, Profarma can develop and validate custom dissolution methods tailored to specific products. Our team works closely with clients to create robust testing protocols that meet regulatory requirements and product specifications.
What types of products can Profarma test for dissolution?
Profarma can perform dissolution testing on a variety of pharmaceutical products, including:
- Immediate-release tablets and capsules
- Extended-release formulations
- Orally disintegrating tablets
- Suspensions
- Transdermal systems
- Specialty dosage forms
How can I get started with Profarma’s dissolution testing services?
To begin, contact Profarma through our website. Our team will discuss your specific needs and provide a tailored proposal for dissolution testing to ensure your product meets all safety, efficacy, and quality standards.