Building a comprehensive evidence-base around product characterisation is essential to optimize your assets for strong clinical performance and successful market authorisation.
Stemmatters can support the design and definition of product specifications to build a well-defined and controlled product that can be consistently manufactured.
We have a strong track record of seamless technology transfer procedures, assuring the ability to validate your optimised solutions in-house.
Stemmatters is able to contribute formulation development, stability studies, biocompatibility studies, and other IND-enabling studies to optimise the product profile of your therapeutic’ for clinical evaluation and commercial success
Process development should ensure full cGMP compliance, remove extraneous handling steps, optimise cost-of-goods, while providing adequate scalability to serve foreseen commercial demand.
Crucially for cell and tissue products, manufacturing processes should be established in such a way that major alterations are not required in late-stage clinical development, which could undermine product’s viability.
Stemmatters specialises in taking early stage product processes through to commercially relevant and scalable manufacturing processes.
We have a successful track record of developing, validating and optimising single-use closed processes that deliver the specified product profile, maintaining quality attributes for products used in non-clinical and clinical applications.
Refining product specifications usually requires the development or application of additional analytical procedures, either to improve analytical capabilities, or for the addition of new ones.
The quality programme of a product requires well-defined and robust specification parameters, in addition to regulatory conformance
Further to product characterisation, process analytical technologies can also be implemented to measure and control manufacturing processes further upstream.
Stemmatters understands the critical importance of the analytical framework, and offers a full-spectrum of analytical development and implementation services, both for product and process to ensure quality and purity of products according to GMP guidelines, including methods for to assess product stability and support end-product release.