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Our analytical services are designed to support your drug development and manufacturing needs with precision and reliability.
Analytical Method Development and Validation: Tailored methods to ensure accuracy, specificity, and reproducibility.
Stability Studies: Comprehensive testing to assess product stability under various conditions.
Raw Material Analysis: Ensuring the quality and consistency of starting materials.
Finished Product Testing: Verifying the safety, efficacy, and quality of final products.
Impurity Profiling: Advanced techniques for identifying and quantifying impurities, including nitrosamines using LCMS.
Elemental Impurities Analysis: Compliance with ICH Q3D guidelines using in-house ICPMS technology.
At the heart of our CDMO support lies a commitment to:
Discover why we are your ideal partner, delivering unmatched expertise, reliability, and innovative solutions.
Equipped with 21 CFR Part 11-compliant instruments.
Fully compliant with FDA, EMA, and WHO standards.
Efficient processes for fast, reliable results.
Transparent communication and seamless integration with your team.
Request you to provide all details mentioned in the form along with your business requirement. It will help us route your query to the appropriate person.
