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400 Professional Drive , Suite 400, Gaithersburg, MD, 20879, US
Avoid Risks and Delays in Bringing your Drug to Market
Released By Emergent Bioservices
Total baseline value for Emergent is approximately $90 million USD, further expanding the collaboration between the companies, which began in February 2021.
For innovators taking on global health risks, rare diseases, or novel medicines, Emergent is an ideal integrated CDMO and a valued partner.
Lenzilumab™ is currently in a Phase 3 clinical trial evaluating patients hospitalized with COVID-19. Humanigen intends to file for EUA first quarter of 2021.
to Develop Emergent’s COVID-19 Hyperimmune Globulin (COVID-HIG) Product Candidate with U.S. Department of Defense Funding
for Johnson & Johnson’s Lead COVID-19 Vaccine Candidate
in Canton Site and Expand Viral Vector and Gene Therapy Capability
for AstraZeneca’s COVID-19 Vaccine Candidate
in Landmark Public-Private CDMO Partnership for COVID-19 Vaccine Development and Manufacturing
for Johnson & Johnson’s Lead Vaccine Candidate for COVID-19
to Expedite Development of Plasma-Derived Therapy for COVID-19
with Vaxart for their Experimental Oral Vaccine Candidate for Coronavirus Disease
for the Treatment and Prevention of Coronavirus Disease
With Novavax for Experimental Vaccine Candidate for Coronavirus Disease
The company opened a new GMP Pilot Unit to produce liquid and lyophilized injectable forms.
By: Rachel Klemovitch
Advanced technologies and close collaboration maximize yields, safety, and patient access to life-saving therapies.
By: Sarah Springer
Will add further sterile fill/finish capacity over the course of the next year.
By: Charlie Sternberg
For this roundtable, Contract Pharma called upon thought leaders across the pharmaceutical services sector to address “3 Key Trends” impacting the CDMO industry in 2025 and beyond.
By: Tim Wright
The CEO of Woodstock Sterile Solutions discusses strategic investments, blow-fill-seal leadership, and building a future-ready CDMO.
Why the current CDMO model is failing small-batch manufacturing and what needs to be done.
By: Sam Chia
How innovation, advanced manufacturing, and expertise drive success in the evolving CDMO and generics landscape.
By: Jody Chastain
As part of the investment, Emergent would lead U.S. manufacturing and commercialization efforts for four of Rocketvax’s pipeline candidates.
The Baltimore Biologics Drug Substance facility will serve customers across human and animal health market segments.
CDMO leaders talk about navigating a dynamic landscape of innovation and demand.
Navigating the sterile outsourcing bottleneck and how CDMOs must adapt to meet the growing demand for small-batch biologics and flexible fill-finish solutions.
By: Nikki Whitfield
Post-Covid global trends in capacity utilization and constraints. A 10-year retrospective analysis and future-cast in fill-finish services.
By: Eric Langer
Drug-device combination products are easy for patients to use, but they can be difficult for pharma companies to produce. This article addresses the production pain points, and how they can be overcome.
By: Jeremy Guo
Aims to revolutionize pharmaceutical manufacturing with focus on advanced aseptic processing technology.
By: Kristin Brooks
Pozzi, a professional in the field of packaging systems, has more than twenty years of experience.
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