FUJIFILM Diosynth Biotechnologies offers a full suite of CDMO extended services. We offer quality control, analysis and testing required to support the release of the drug substance, drug product, placebo and stability studies.
As a global organization, we have full on-site Quality Control Laboratories in all of our facilities.
High value proposition
Our fill/finish services are designed to deliver the lowest possible risk to patients while maintaining a high value proposition. Fill/finish includes formulation, vial filling, lyophilization, 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 labeling and packaging
FUJIFILM Diosynth Biotechnologies provides reliable and cost-effective labeling and packaging for clinical and commercial products – to ensure that your supply needs are met. Packaging services include primary packaging such as bottle filling, pillow packaging, blister packaging, card blisters and sachets, as well as secondary packaging for solids and injectables.