FUJIFILM Diosynth Biotechnologies offers a full suite of CDMO extended services.
Our drug product services are designed to deliver the lowest possible risk to patients while maintaining a high value product, and include formulation, vial filling, testing / stability testing and release of licensed products.
Partners for success
We deliver a first-in-class Process Characterization (PC) program design and execution to support your product registration and commercialization strategy. Process characterization services can be included as part of your product and process development lifecycle. We also offer process characterization studies as a free-standing service.
Defining a capable manufacturing process
Process Validation is a pivotal lifecycle activity that involves the collection and evaluation of process data and knowledge to establish a defendable control strategy and defines a capable manufacturing process that reliably meets product quality attributes.
cGMP Quality Control is an integral part of the manufacturing process
FUJIFILM Diosynth Biotechnologies offers a full suite of quality control, analysis and testing required to support the release of the drug substance, drug product, placebo and stability studies.
Reliable and cost-effective assembly, labeling and packaging
We provide solutions for clinical and commercial products to ensure that your supply needs are met. Packaging services include primary and secondary labelling for vials and prefilled syringes, serialization, single, multi and blister packaging, plus assembly of auto-injectors.