ElevateBio: Manufacturing Your Vision
We have the expertise, technologies, and state-of-the-art facilities at ElevateBio BaseCamp® for full-scale manufacturing of your therapies.
Our BaseCamp® facility in Waltham, MA is built with multiple segregated manufacturing suites for cell therapy products and viral vectors, designed with flexibility to support development and commercial production needs.
Get in touch with ElevateBio today to start moving your transformative therapies into full production.
From Clinical Success to Commercial Readiness
ElevateBio leads the way for therapies that have completed clinical trials and are now ready for commercial manufacturing. For high-volume demand, ElevateBio has the expertise and facilities to handle full production.
To see how ElevateBio made the transition to full manufacturing, and how our facilities are equipped to handle your needs, view the presentation from CAR-TCR Summit by ElevateBio’s Katie Jorgenson, Site Head at BaseCamp® Waltham.
From BaseCamp to Summit…
BaseCamp® is our genetic medicine current Good Manufacturing Practice (cGMP) manufacturing and process development business enabling biopharmaceutical partners with end-to-end capabilities.
The purpose-built viral vector and cell therapy centers of excellence provide the tools, expertise, and resources necessary to bring these advanced therapies from concept to commercialization.
We are leading the revolution in cell and gene therapy development, first through our flagship BaseCamp facility in Waltham, Massachusetts and beyond as we expand to new intersections of science, technology, and talent.
Explore What’s Inside BaseCamp
BaseCamp® provides the technologies, expertise, operations, processes, and manufacturing capabilities to accelerate the development of life-transformative advanced therapies. Our 140,000 square foot flagship cGMP process development facility is located in Waltham, MA and provides:
- End-to-end solutions for cGMP manufacturing, warehouse and distribution capabilities
- Automated systems for real-time review of process data and release of product
- Support across a range of CMC regulatory activities
GMP Manufacturing
- Grade B and C BSL2 Cleanrooms
- 3 viral vector suites (+ host cell & fill/finish)
- LVV and AAV production
- 6 cell therapy suites
- Once-through HVAC
R&D and QC Laboratories
- Biosafety level 2 classification
- Onsite QC support for batch release
Utility and Support Space
- Segregated clean and building utility rooms
- Water for injection loop
- QA document storage room
Warehouses
- Segregated GMP and non-GMP warehousing
- Validated cold storage and monitoring
Office & Support Spaces
- ~200 employees
- Conference/huddle/amenities
Ready to Get Started?
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