Comprehensive analytical services and capabilities
Our highly-experienced team uses a wide array of innovative analytical techniques to validate all raw materials, bulk solutions, in-process materials, and finished products. Our highly trained analytical quality control staff also provides support for the critical transfer of analytical methods.
Vetter offers qualification, analysis, and release of the starting materials necessary for compounding of your drug product.
In-process samples, release, and stability testing
During early clinical development, we support you with a wide range of analytical services aligned to streamline quick-release analytical testing of your clinical material including chemical, biochemical, and microbiological testing for in-process samples, release, and stability testing.
We work with you to validate chemical and microbiological methods and to transfer your validated product-specific microbiological and chemical analytical methods in house. This provides a seamless transition to clinical manufacturing and allows you to formally release your batches.
Our service includes storage and testing of stability samples according to ICH conditions, accommodating both standard temperature ranges and custom requirements.