Analytical Chemistry
Outsourced Testing- Analytical Chemistry
At ATL, a Bureau Veritas Company, our contract testing laboratory supports all phases of the product lifecycle.
We have a wealth of experience assessing raw materials, active ingredients, process intermediates, and finished products, from research through commercialization.
We provide high-quality testing, results, and data across a wide range of technologies and applications for all phases of development and manufacturing. If you’re bringing pharmaceutical, personal care, consumer goods or medical device products to market, our guidance can help you navigate the regulatory and compendial guidelines.
Examples of Testing Capability– Analytical Chemistry
Our experience with method development and feasibility crosses multiple industries and technologies and encompasses optimization, validation, transfer and verification. We follow compendia methods (USP, EP, JP), client-supported methods and methods we’ve developed and validated for clients. Additionally, our capabilities and expertise support both instrumentation and wet chemistry including:
- In-Process and Product Release Testing and Retain Program Administration
- Stability Testing and Stability Indicating Method Development
- Comparative Product Testing
- Raw Material Testing (USP / NF, EP, JP)
- Quality Control Release Testing
- Impurities Testing
- Assay/Potency determination
- Cleaning validation analysis
- Extractable/leachable testing
- Residual solvents
- Elemental metals
METHOD DEVELOPMENT & FEASIBILITY
We apply Quality by Design principles to all method development phases.
METHOD VALIDATION
We validate all methods with applicable regulatory requirements and validations are always performed under a pre-approved protocol.
METHOD VERIFICATION
We offer significant experience in compendia verification methods and method transfer situations and perform verifications under a pre-approved protocol.