Description
Welcome to N.H.P. Laboratories, your premier partner for dissolution testing services tailored to meet the needs of the natural health–product and pharmaceutical industries. As an ISO 17025–accredited laboratory, we are dedicated to delivering precise and dependable dissolution-testing results for your formulations. Trust us to ensure the efficacy, quality, and regulatory compliance for your products.
We offer a comprehensive suite of dissolution testing services designed to optimize the performance and compliance for your formulations. With our ISO 17025 accreditation and commitment to excellence, you can trust us to deliver accurate and reliable results every time. Whether it is for dissolution-profile analysis, method development, or stability studies, our experienced team provides personalized solutions to meet your specific needs. Partner with us to ensure the quality, efficacy, and regulatory compliance for your products.
Key Tests
- Dissolution Profile Analysis: Evaluation of the release kinetics of active pharmaceutical ingredients (APIs) from solid dosage forms under standardized conditions.
- Dissolution Method Development: Customized dissolution methods tailored to your specific formulation characteristics and regulatory requirements.
- Dissolution Stability Studies: Assess the stability of pharmaceuticals by monitoring dissolution profiles over time under various storage conditions.
Case Studies or Testimonials
Discover success stories and testimonials from clients who have leveraged N.H.P. Laboratories for dissolution testing. Learn how our expertise and dedication to accuracy have contributed to the success of their natural health–product and pharmaceutical development projects.
Why Choose N.H.P. Laboratories for Dissolution Testing?