Biologics to the market can be a challenging and time-sensitive process.We adhere to R&D, GMP and GLP guidelines, committed to providing the best possible service and individual care, including dedicated project managers, to accelerate the development of your biologic from discovery testing through to product release. We offer constant and relevant communication to ensure that clients are informed every step of the way to help you plan, anticipate and navigate through the challenges of bringing a biological product to market.

We can evaluate candidate products for large clients as well as clients with limited capacity or resources in-house and other consulting services, include adjuvant assessment, assay design development and validation, efficacy testing and assessment of different routes of administration. Our partnership Charles River has over 15 years of experience in method development. Which can support you in meeting novel or changing requirements with assay design, development, optimization and validation, as well as routine testing.