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12601 Twinbrook Pkwy., Rockeville, MD, 20852
The first in a planned series of guides, launched in August 2023, covers control strategies for continuous manufacturing of solid oral dose drugs.
Released By U.S. Pharmacopeia (USP)
Learn about USP products and solutions including USP reference samples, Compounding Compendium, Dietary Supplement Verification, education courses and more.
In case you missed it, USP officially launched the Continuous Manufacturing Knowledge Center (CMKC) – an online platform that captures, organizes, and updates rapidly expanding knowledge about continuous manufacturing and fosters a community network where experts can collaborate to close the knowledge gap. Within this community, there are groups focused on specific topics such as Continuous […]
Reducing barriers to advanced manufacturing.
Public standards, R&D analytical solutions, consulting and training.
Explore our services to learn why we are the standard of trust.
As a company producing Oral Solid Dose drug products, how can Pharmaceutical Continuous Manufacturing solve specific problems and help your business thrive?
Will help enable broader adoption of advanced manufacturing technologies and state-of-the-art quality solutions
By: Charlie Sternberg
ATP-bioluminescence and regulatory advancements address unmet manufacturing and testing needs.
Key steps for pharmaceutical companies to meet FDA’s upcoming nitrosamine testing requirements and ensure product safety.
By: Joshua Hoerner, Amber Burch
Ginkgo Bioworks gains a $29 million contract by ARPA-H to develop distributed manufacturing of essential medicines using wheat germ cell-free expression systems.
By: Rachel Klemovitch
The characterization of product-related variants in monoclonal antibodies involves identifying and quantifying the size and charge of variants that can impact..
Released By Bora Biologics
Twelve months on from its acquisition of Qualicaps, the company remains at the forefront of innovation.
Exploring the case for softgels and CDMO partnerships with Peter Surman, Chief Scientific Officer at Douglas CDMO.
Released By Douglas CDMO
Exploring best practices for the employment of quality risk management within laboratory operations.
By: Paul Mason
Insights from the regulatory experts at Lachman Consultants.
By: Tony Polletta
The event will see some 58 sessions with several notable keynotes.
Enter a collaboration and co-marketing agreement to reduce protein interference in bacterial endotoxin testing of biopharmaceutical products.
Evaluating extractables and leachables, overseeing manufacturing processes, ensuring adherence to CGMPs and comprehensive packaging testing.
By: Sandi schaible
To create a pharmaceutical packaging bottle manufactured with 100% recycled virgin quality Loop PET resin.
By: Kristin Brooks
Back to the future in analytical methods.
By: Emil W. Ciurczak
The new world of Environmental, Social, and Governance (ESG) investing is now a top concern for the pharmaceutical industry.
By: Andrea Sentimenti
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