
Your Science.
Our Manufacturing Power.
One Seamless Path.
The right Contract Development and Manufacturing Organization (CDMO) partner doesn’t just make your product—it accelerates your success. At SCTbio, we deliver expertise, flexibility, and scale for every stage of your cell and gene therapy journey. Backed by PPF Group, we combine world-class manufacturing with seamless execution.

Measured in Results.
Proven in Impact.
~20
years
manufacturing cell & gene therapies
3
Qualified Persons on Site for agile batch release

150+
legacy EU/US qualified apheresis sites — unmatched expertise in clinical collection management
2,000+
GMP batches manufactured
2,000 m²
of advanced facilities, including 420 m² of Class A/B/C GMP cleanrooms
12,000
IMPs delivered worldwide
75+
cell therapy experts dedicated to your success
End-to-End Solutions.
Built for Your Therapy.
From bench to bedside, SCTbio offers full-service support for Advanced Therapy Medicinal Products (ATMPs):

cGMP Manufacturing and Quality Control
Cell therapy and viral vector
expertise with robust in-house QC capabilities

Lentiviral & Gammaretroviral Vector Production & Testing
Viral vectors development and manufacturing - scalable RUO & GMP grades

Analytical
Development
Analytical development include
method development,
optimization, and validation

Process Development & Tech Transfer
Scalable, optimized processes
with successful transfer from lab to GMP

Apheresis Collection
& Logistics
Seamless needle‑to‑needle coordination across 150+ EU/US legacy apheresis sites — from apheresis to patient delivery

Storage
& Distribution
Proprietary global GxP logistics, controlled storage, and cold chain management

Quality & Regulatory Support & Qualified Person Services
QP batch release under EU GMP and global compliance support
What Our Partners Say About Us
Extensive Global Heritage in Apheresis Management
SCTbio draws on a long-standing legacy of working with more than 150 qualified and trained cell-collection sites across Europe and the USA. We provide dedicated apheresis support, with rapid reactivation and site‑specific procedure alignment to secure high‑quality clinical starting material.



