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115 West Century Road, Suite 340, Paramus, NJ, 07652, US
Tablet lubricants play a key role in pharmaceutical manufacturing, affecting everything from compression behavior to tablet performance and regulatory compliance. If you’ve ever faced challenges with API compatibility, over-blending, or mitigating nitrosamine risks, it may be time to explore safer, more robust alternatives. This in-depth whitepaper discusses common challenges in tablet lubrication and introduces Compritol® 888 […]
Released By Gattefossé USA
Platform and product releases span OPUS, MINT, POET, and SPI.
By: Rachel Klemovitch
Will expand domestic active pharmaceutical ingredient (API) production in the U.S.
By: Charlie Sternberg
Williamson offers experience building innovative life sciences companies and delivering strong commercial and operational outcomes.
New alliance is dedicated to advancing lipid nanoparticle (LNP) technology and accelerating the development of next-generation therapeutics.
The site is also expanding its High Potency Active Pharmaceutical Ingredient and Antibody Drug Conjugate capacity.
Collaboration complements Bayer's precision oncology development portfolio in the areas of pancreatic, colorectal, and lung cancer.
Avista will leverage Forge’s FUEL platform to manufacture AAV for AVST-101, Avista’s lead gene therapy to treat patients with X-linked retinoschisis (XLRS).
Collaboration aims to scale OBD's analytical framework by leveraging Google Cloud's infrastructure.
Certifies ElevateBio’s compliant and scalable manufacturing capabilities for advanced therapies using U.S. and E.U. commercial-level evaluation standards.
The new facility designs, develops and manufactures research-grade pDNA materials to support the cell and gene therapy field.
Sartorius supports commercialization and joint development of solutions based on Nanotein’s NanoSpark platform.
If approved, gepotidacin would offer a new oral option to U.S. patients currently relying on injectable treatments for uncomplicated urogenital gonorrhea.
AVTOZMA IV now aligns with all indications approved for ACTEMRA IV in the United States.
Strategic expansion is designed to advance gene therapy development and manufacturing.
CureVac and GSK will receive $740 million and single-digit royalties on COVID-19 vaccine sales in the U.S. going forward.
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