The program is still filling in: some talks have no title yet and more speakers will be added. We’ll add new sessions, the organizations presenting them and stand numbers once the floor plan is published.

Biosimilars, regulation and access at Festival of Biologics USA 2027

Apr 13–14, 2027 Boston, MA ~2k attendees Website

10 organizations at Festival of Biologics USA 2027 present work in biosimilars, regulation & access: 4 suppliers and service providers, 3 academic, government and non-profit bodies and 3 drug developers. Between them they bring 9 presentations to the program. Most represented: UC San Diego, Access to Medicine Foundation and American Oncology Network. As of Oct 15, 2026.

All 126 organizations at Festival of Biologics USA 2027 →

Format
Top represented
Showing 1–10 of 10 organizations
OrganizationFestival of Biologics USA 2027 Attendance
UC San Diego
San Diego, CA
Talk
Tue Apr 13
13:50
Bioprocessing to make biosimilars accessible
Biosimilars
Talk
Tue Apr 13
16:40
Leveraging AI in Computational Medicine
AI & Data
Access to Medicine Foundation
Amsterdam, Netherlands
Gov/NGO
Non-profit that analyzes how pharmaceutical companies improve access to medicine in low- and middle-income countries.
Keynote
Tue Apr 13
09:10
Making high impact decisions across the value chain to effect access and affordability
Keynotes
Biosimilars, regulation & access
Consulting & services
Network of community oncology practices, supplying them with practice management, pharmacy and value-based care services.
Talk
Tue Apr 13
12:00
Talk
Tue Apr 13
15:10
Analytical development and characterization of biosimilars
Biosimilars
Ipca Laboratories
Mumbai, India
Large pharma
Makes and markets finished formulations and active pharmaceutical ingredients, and develops biosimilars.
Talk
Tue Apr 13
14:30
Ensuring High Biosimilarity Through Advanced Processes and Characterization Approaches
Biosimilars
Biotech
Develops biosimilars and complex generic medicines; acquired by Amneal Pharmaceuticals in 2026.
Talk
Tue Apr 13
16:40
Streamlined Development: 2-year perspective what's changed
Why regulators now let biosimilars, near-copies of existing biologic drugs, skip comparative efficacy trials, shifting the focus to detailed lab comparisons.
MJH Life Sciences
Cranbury, NJ
Consulting & services
Healthcare media company publishing clinical news, journals and events for physicians, pharmacists and life science companies.
Talk
Tue Apr 13
11:00
Orchard Therapeutics
London, United Kingdom
Biotech
Develops hematopoietic stem cell gene therapies for severe rare diseases; part of Kyowa Kirin.
Talk
Tue Apr 13
11:40
Launching a biosimilar: the US landscape for biosimilar products
Biosimilars
ProductLife Group
Paris, France
Consulting & services
Consultancy providing regulatory affairs, pharmacovigilance, quality, market access and engineering services across the product lifecycle.
Booth
Exhibiting (no floor booth listed)
Software & AIGold sponsor
AI platform for drafting and managing regulatory submissions and health authority questions, keeping dossiers linked to source data.
Booth
Exhibiting (no floor booth listed)

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