Accelerate Your
Cell & Gene Therapy
Contract Development & Manufacturing
Accelerate Your
Cell & Gene Therapy
Contract Development & Manufacturing
At NecstGen, we enable the next generation of therapies by offering development support and GMP production of Cell and Gene Therapies. Together, we challenge today’s possibilities and enable the unthinkable.
Are you bringing a Gene or Cell Therapy to patients? We can help.
Solely dedicated to the field of Cell and Gene Therapy, we provide capacity, expertise, and services tailored accelerate the development of your therapy to the clinic and beyond. Our approach is characterised by open and transparent communication, fostering a culture of collaboration and knowledge sharing.
Cell Therapies
NecstGen offers services for Cell Therapy and ex vivo Cell Therapy process and analytical development and manufacturing.
Viral Vectors
NecstGen provides a high-caliber process for Viral Vector manufacturing for your Gene Therapy.
Consultancy & Support
NecstGen offers consultancy and support throughout all stages of therapy development .
“At NecstGen, we offer process development solutions, contract preclinical/ GMP manufacturing and consultancy for Cell and Gene Therapies to clinicians, academic, small, medium, and large commercial organisations worldwide. We have a focused expert team and bespoke facility to offer you the support and capacity needed to deliver your therapy to patients.
We enable the next generation of therapies by translating research programs into health solutions for patients.“
News & Insights
Niek Visarius joins NecstGen as Interim CEO and Transition Manager
Leading NecstGen’s integration into LUMC while ensuring continuity across its programs and services.
Webinar Replay: ‘Case Study: Development of a Scalable LV Production Platform’
Learn how structured process development can support scalable lentiviral vector production.
The Details Decide Everything: Melissa van Pel on Translating Cell Therapy
Moving a cell therapy from bench to patient rarely fails because of one large mistake. It stalls because of dozens of small, unspoken assumptions about what a manufacturing process should look like, what regulators will accept, and when a process is truly ready.





