Drug product, CMC and tech transfer for biologics and cell therapy.
Deben Bioprocess supports start-ups and scale-ups with practical manufacturing solutions: GMP fill-finish, PPQ protocols, and cell therapy launch readiness. Hands-on engineering. Clear strategy. No jargon.
Named for a Suffolk river. Built on manufacturing experience.
The River Deben runs quietly through Suffolk. It is deep, reliable, and patient. Deben Bioprocess works the same way: practical GMP engineering, clear CMC strategy, and hands-on MSAT support delivered without jargon, in step with what your programme actually needs.
Hands-on support for drug product manufacturing, from development to commercial launch.
- PPQ strategy and protocol writing
- Stability and shelf-life planning
- Batch record review and release
Cross-functional CMC leadership and regulatory readiness for biologics and ATMPs.
- Regulatory submission authoring
- Health Authority response support
- CMC lifecycle and IP strategy
Transfer of bespoke processes into CMOs or internal sites with a platform-first approach.
- CMO selection and technical oversight
- Scale-up and process fit assessment
- Gap analysis and remediation plans
Need drug product or CMC support?
Short engagements, retained advisory, or full project support. Tell us what you are working on.
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