Viral vector production platforms: Flash facilities
Our state-of-the-art industrial facility is designed to meet the rigorous demands of viral vector production. As a leading CDMO, Flash BioSolutions offers a comprehensive range of capabilities to support your project from concept to clinical application.
World-Class cGMP manufacturing facility
French cGMP manufacturing facilities for worldwide delivery of your viral vector batches. Our facilities are fully compliant with both American and European GMP guidelines, ensuring the highest standards of quality and safety for your therapeutic products.
Our CDMO services
- Construct and plasmid design
- Process development
- R&D production
- GMP manufacturing
- Analytical method development
- Fill & Finish
- QA release
- Stability studies
- Regulatory support – CMC section
CDMO CAPABILITIES FOR GMP VIRAL VECTOR
Our GMP facility can produce up to 40 batches per year, ensuring that we can meet your production needs efficiently and reliably. With a focus on quality and precision, Flash BioSolutions is your partner in advancing therapeutic innovation.
Our state-of-the-art facilities, coupled with our extensive expertise, position Flash BioSolutions as a premier choice for viral vector production. We are committed to delivering excellence at every stage, from initial construct design to final product release, ensuring the success of your clinical studies and therapeutic programs.
Our STATE-OF-THE-ART FACILITIes
At our integrated facilities, we offer both R&D grade and GMP grade manufacturing environments to support the full spectrum of biopharmaceutical development and production needs.
R&D laboratories
Our R&D grade manufacturing facility spans 1200m² of BSL2 laboratories, designed to support comprehensive research and development activities.
- Area for quality control activities
- Area dedicated to cell culture, and cell line development
- Area dedicated to vector manufacturing including process development
- Storage areas
GMP Facility
Our GMP grade manufacturing facility encompasses 1000m² of high-standard cleanrooms, essential for Good Manufacturing Practice (GMP) compliant operations.
- Independent and separate suites in B class (cell culture and expansion, media preparation, fill & finish)
- Independent suites in C class dedicated to vector manufacturing (Upstream, Downstream)
- Storage areas (-80°C, -150°C)
Storage areas:
CONTACT US
We invite you to reach out to us for any inquiries regarding our services, technical support, or potential collaborations.
Please complete the following form, and a member of our team will respond promptly.
+33(0) 5 61 28 70 75
