Explore how we’re accelerating what's next in advanced therapies and how we can serve as your strategic partner for mRNA and viral vector programs.
September 22–25, 2026 | Boston, MA
BioProcess International 2026—taking place September 22–25 in Boston, MA—will spotlight breakthroughs shaping the discovery, scale-up, and delivery of advanced therapies across five core pillars. The program features keynotes, sessions, workshops, and case-study forums that deliver practical strategies to improve quality, shorten timelines, and increase efficiency from early development through commercialization.
From cell line development and engineering to upstream processing and cell culture, downstream processing, digital biomanufacturing and data-driven operations, and CMC strategy and manufacturing performance, this event will cover a myriad of challenges facing drug developers today. Come discover how our integrated services and solutions can help you overcome obstacles and reduce risk on your journey to market.
Date: September 22–25, 2026
Format: In-person
Location: Hynes Convention Center, Boston, US
Event website: BioProcess International (BPI) | Conference and Exhibition | Official Event Website
Advanced therapies utilizing next-generation technologies such as mRNA and viral vectors are set to change the biopharmaceutical industry as we know it. As a leading CDMO and CRO partner, we’re excited to be at the forefront of innovation in this field, supporting our drug development partners through every phase of the journey to market—from early development through scale-up, manufacturing, and commercialization.
Through collaborative partnerships with biotechnology and pharmaceutical companies, we are helping accelerate what’s next in advanced therapies. By combining scientific expertise, trusted guidance, and proven execution, our end-to-end offerings help transform possibilities into products that benefit patients in need around the globe. We look forward to showcasing our capabilities at BioProcess International (BPI) 2026.
Lentiviral vectors (LVVs) are critical for ex vivo and emerging in vivo gene therapies, yet scalable manufacturing remains limited by low infectious yields, process variability, and the need to balance vector recovery with impurity clearance. We developed an integrated manufacturing platform that combines high-throughput upstream process optimization with scalable downstream purification to address these challenges.
Join this presentation to learn how:
Session details:
Schedule a meeting with Thermo Fisher Scientific at BioProcess International (BPI) 2026 to explore our integrated CDMO and CRO offerings, including services and solutions for mRNA and viral vector advanced therapy programs.
We look forward to seeing you soon.
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