Your CDMO for Life-Changing Therapies.
The human link between your science and patient's story.
 | FDA & EMA APPROVED |
Dedicated expertise that turns biological breakthroughs into a patient's reality.
From cell line development with Sartorius to GMP manufacturing : one integrated program, built around your molecule.
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Explore our capabilities
 Cell Line Development Sartorius × LFB : best-in-class CLD expertise fully integrated with GMP manufacturing : one program, two specialists. |
 Process Development USP/DSP optimization from Ambr™ microscale to 50 L pilot — with DoE methodology and seamless tech transfer to GMP. |
 GMP Capabilities Clinical & commercial batches — 100+ GMP batches delivered, 200 L to 2 000 L single-use technology, FDA-approved since 2020. |
Quality & Regulatory Audit-ready quality system, FDA & ANSM track record — full CMC support for your IND, BLA, or MAA submission. |
LFB Biomanufacturing: Delivering Results, Backed by Experience
A CDMO trusted by Global Biotech Innovators
 Sartorius × LFB Biomanufacturing : two specialists, one integrated program
Better than a one-stop-shop — two specialists, zero compromise.
Sartorius brings world-class CLD expertise. Together: best-in-class at every stage, with the simplicity of a single program. |
Among Many Global Biotech Leaders
CDMO experts dedicated to your program
The human link between your vision and clinical success.
Dedicated multidisciplinary teams, clear project governance, transparent planning — a CDMO that stays human at scale. We bring together science, engineering and quality expertise under one roof, ensuring every project receives the attention and agility it deserves.
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Ready to discuss your project?
Your molecule deserves the best of both worlds – Sartorius CLD expertise and LFB GMP manufacturing.
Let’s build your program together. |
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