Leading-Edge Analytical Solutions for the Pharmaceutical Industry
We offer a wide range of analytical development services to support the pharmaceutical industry. Our state-of-the-art analytical laboratories are equipped with sophisticated instruments that comply with 21 CFR Part 11 standards, allowing us to deliver accurate, reliable, and high-quality data.
Advanced Testing Capabilities
Our analytical services include analytical method development and validation, stability studies, raw material analysis, finished product testing, and impurity profiling. We also have the capability to analyze nitrosamine impurities using LCMS and to comply with upcoming ICH Q3D requirements of “Elemental Impurities” with in-house “ICPMS.”
Compliant and Quality-Centric Approach
All our analytical services are performed in strict accordance with Good Laboratory Practices (GLP) and comply with national and international regulatory requirements. Our commitment to quality ensures reliable and consistent results.
Expert Team
Our team of seasoned analytical chemists brings together extensive industry experience and a deep understanding of analytical method validation in pharma. They work collaboratively with clients, offering expert advice and delivering solutions that meet their unique needs.
Commitment to Timely Delivery
We understand the critical role of analytical services in pharmaceutical development and manufacturing. Our efficient processes and dedicated team ensure that our analytical services are delivered on time, every time.
Partnering for Success
We work as an extension of our clients’ teams, providing transparent, regular updates at every stage of the analytical process. Our partnership approach ensures a seamless experience and successful outcomes in pharmaceutical method validation.
