Center for Cell and Gene therapy
Services
We offer end-to-end support for the development and manufacturing of cell and gene therapies and infectious challenge agents. This includes GMP production of ATMPs and challenge agents, translational process development, regulatory support, and quality control testing. Whether you are an academic researcher, clinician, or other partner, we help you move your therapy toward the clinic. From the first idea to a release-ready product, our team guides you through every step. Visit the Services page to learn more.
Equipment
The Good Manufacturing Practices licensed (GMP-licensed) Cleanroom Facility has 6 class A in B cleanrooms , fully equipped with the standard equipment necessary for the production of cell and gene therapy products. Along with the standard equipment, we also offer specialised equipment, such as bioreactors, for the manufacturing of ATMPs or other innovative biological products.
Quality assurance
The facility has a GMP license (Certificate NL/H 21/2029320B) for the production and batch certification of cell therapy, gene therapy and tissue engineered products.
About us
The Center for Cell and Gene Therapy Facility supports the development and production of ATMPs and other innovative medicinal products.
Our team
- Pauline Meij, Clinical bioacademic staff member, QC, QP, Head of CCG
- Inge van Amerongen-Westra, Clinical bioacademic staff member, QC, QP
- Eileen van der Stoep, Hospital pharmacist, QP
- Helene Roelofs, Clinical bioacademic staff member, QC, QP
- Mara Tihaya, PostDoc researcher
- Fong Lin, Research technician
- Susanne Kortekaas, Research technician
- Natascha Fonseca Neves, Research technician
Contact
Contact
+31 71 5264177
CCG@lumc.nl
Address
Location J-10-090
LUMC building 1
Albinusdreef 2
2333 ZA Leiden