WELCOME TO VINTABIO

Vinta Bio delivers customized process development
and GMP manufacturing service for cell and gene therapy.

about us

YOUR ACHIEVEMENT IS OUR MISSION

From concept to success, from one to many.
We are here for you at every step of the way.

get in touch

Our one-stream process

Offers consistency and transformability at every stage of your vector needs.

Research Vector Service

Analytical Service

GMP Production

Regulatory Support

Research Vector

Analytical Service

GMP production

Regulatory Support

Centered around viral vector product releases, our analytical services center around biological assays that are essential for viral vector quality control. From assay transfer to assay qualification and validation, our analytical team is ready to assist. Our goal is to make your ideas a reality.
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How We Can Work Together

GMP Manufacturing

CGMP QC Services

Plasmid Manufacturing

AAV

For delivering gene therapeutics

Lentivirus

For delivering gene therapeutics 

FAQ

Vinta’s package helps you turn your concept into success at every step of the way, from research to clinical research viral vectors. We offer consistency and reliability by using the same master cell bank and production plasmids. Coupled with a strong analytical team and a semi-automated filling station in a dedicated fill room, Vinta’s one stream viral vector package have you covered from proof of concept to clinical trial in gene therapy product development.
At Vinta, we offer vector production at multiple different quality scales:

- Research Use Only (RUO) vector material
- “GMP-like” material
- cGMP material

Research Use Only (RUO) vector material is typically generated at a controlled research lab with dedicated production team. Although the production process is consistent, it is not controlled, recorded, or reviewed by our quality team.

Our “GMP-like” material is produced at dedicated research or monitored cleanroom environment, and the production process is recorded. Depending on your needs, various aspects of the production process can be controlled and reviewed by our QA group, including the final product release.

Our cGMP material is produced at dedicated, monitored ISO-7 environment. All material used for production go through review and release process and is dedicated the batch.

Our quality management system is involved in every step of the production from batch record issuance to deviation resolution, and batch release. With a dedicated filling station suitable for clinical trial material and strong analytical support, our GMP vector production service is full spectrum.
Each request is individual, unique, and special. We have found that the quickest way to get things started is to give us a call. We can address your questions and find the right level of service in a more personalized manner with a one-on-one chat.

CONTACT US

Find out how our team can help your viral vector needs