DEVELOPMENT SERVICES

Analytical Methods Development

Northway Biotechpharma’s quality control team provides high-quality analytical method development services.

We have full analytical capabilities to employ a variety of advanced techniques to elucidate the physical and chemical characteristics of the expressed proteins. Our analytical activities are conducted in-house, allowing us to characterize, monitor and optimize your product’s quality attributes across all stages of development.


Analytical Development Capabilities

  • Liquid chromatography (SEC, RP, IE, and HIC HPLC) analytical method development, qualification and validation
  • Development, qualification and validation of capillary gel electrophoresis, icIEF, SDS-PAGE and other protein purity methods
  • Analysis by UV-Vis spectroscopy, ELISA, Octet, RT-PCR and Biacore
  • Subvisible particle analysis by compendial light obscuration and MFI methods
  • Elucidation of protein structure by LC-MS/MS
  • Development, qualification and validation of cell-based biological assays

DEVELOPMENT SERVICES

Cell Line Development

We offer the flexibility of both mammalian and microbial expression systems – and the expertise to develop the optimal cell line for your product.

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DEVELOPMENT SERVICES

Process Development

Our R&D experts work with you to develop processes that can be efficiently transferred and seamlessly scaled up for production.

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DEVELOPMENT SERVICES

Formulation Development

From the earliest stages of development, we are committed to ensuring the long-term safety and efficacy of your product in the finished dosage form.

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