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| Analytical Testing Services |
Boston Analytical has been performing world-class Analytical Development - Validation and Analytical Chemistry testing for the Pharmaceutical industry, in support of CMC drug development, for over 20 years. Our seamless methods and systems produce high-quality data that is proven reliable and meets industry regulatory requirements. At every step of the process, Boston Analytical is there working with you to evaluate fundamental milestones and to determine the most effective course of action and timeline to meet all of your expectations.
Analytical Testing Services
We would be glad to partner with you on:
- Method Development and Validation
- USP Testing
- In-process and Lot Release Testing
- Raw Material Testing
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Analytical Testing Processes and Methods
Our innovative and intelligent analytical testing processes and methods are time-tested and proven to meet all the demands of potency, purity, and stability:
Analytical Testing Processes
- Stability Indicating and Robust
- Method Transfer
- Impurities / Degradation Products
- Method Evaluation / Optimization
- Cleaning Validation
- Process Validation
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Analytical Testing Methods
- Assay / Purity
- Impurities / Related Compounds
- Finished Product Release
- Dissolution Apparatus I, II, III & V
- Disintegration
- Drug Release Profiles Automated Sampling
- Residual Solvents <467>
- Atomic Absorption
- HPLC / GC with Various Detectors
- Ion Chromatography
- USP Monograph Testing
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FDA cGMP Compliant Laboratory
Boston Analytical’s analytical testing services department is a state-of-the-art FDA, cGMP compliant laboratory. We continually invest in the latest equipment and technology available to provide you with precise, efficient, and timely analytical testing services.
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