Analytical Methods

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At Selvita, we understand that robust and reliable analytical methods are critical to the success of drug development. Our approach to analytical method development, optimization, qualification, and validation is rooted in our extensive expertise and commitment to excellence. Here's how we ensure that our analytical methods meet the highest industry standards: Method Development: · Purity Determination and Assays · Parameter Evaluation Method Optimization: · Current Standards Compliance · Improved Performance Method Validation: · Adherence to ICH Guidelines · Comprehensive Documentation Method Verification: · Limited Parameter Testing · Adherence to Protocols Method Transfer: · cGMP Compliance · Experienced Supervision
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Analytical Methods (Biopharmaceutical Products)Development & Validation of Analytical Methods
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Biopharmaceutical ProductsContract Development and Manufacturing Organisations (CDMOs) and Contract Manufacturing Organisations (CMOs) (Services)
Selvita S.ASelvita is a Contract Laboratory providing multidisciplinary support in resolving the unique challenges of research within the areas of drug development for small molecules and biologics. Selvita was established in 2007 and currently employs over 1,000 professionals, of which over 40% hold a PhD degree. The Company research sites are located in Krakow (HQ) and Poznan, Poland, as well as Zagreb, Croatia. Selvita's international offices are located in Cambridge, MA, and the San Francisco Bay Area in the U.S.

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