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The life sciences tools and services company said U.S.-China tariffs are expected to cut 2025 revenue by $400 million and adjusted operating income by $375 million.

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The CDMO plans to build and expand small, medium, and large manufacturing facilities across Europe and the U.S. over the next three years to meet rising demand for peptides.
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The CDMO, with 3,200 employees at 20 locations in the U.S., Europe and India, has a global footprint to help customers navigate their R&D and manufacturing challenges.
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The company says it is investing in areas across the value chain to ensure its customers continue to enjoy the benefits of a global network with local access.
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Despite Trump’s efforts to bring manufacturing back to the U.S., the threat of tariffs is accelerating an ongoing move to regional redundancy and capacity distribution.
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The White House on Wednesday said pharmaceuticals are exempted from the reciprocal tariffs. Jefferies analysts called the impact on biopharma “minimal” at least for now.
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Pharma Manufacturing sat down with Christian Seufert, Lonza’s Head of Advanced Synthesis, which represents about 30% of the CDMO’s revenue.

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Editors' (re)View

Weekly takes on things going on in the pharma world.

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In the pharmaceutical industry, the pressure to produce high-quality products and remain competitive has never been greater. The rising costs of drug manufacturing and the increasing...
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What’s next for pharma manufacturing in 2025? As the industry continues to respond to new scientific breakthroughs, supply chain pressures, and geopolitical tensions, the...
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Learn how to overcome challenges in pharmaceutical engineering.
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Enable full visibility and optimization of operations by utilizing continuous, actionable insights.
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Learn about the urgent challenges the pharma industry is facing.
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Pharmaceutical manufacturing operates in a high-stakes environment where regulatory compliance, product integrity, and operational uptime are non-negotiable. As the industry becomes...

With a focus on CGT manufacturing, BioForge will be operational by 2027.
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The future of non-clinical research may depend on integrating VCGs for a more humane and efficient approach.
A look at consequential drug approvals and rejections from this year
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With key players entering the ring and many clinical trials underway, the molecular glue garden is bound to bloom soon
A first-of-its-kind study of isotopic values of paired reactants and products offers a prospective new method of process understanding

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Adhering to a tried-and-true set of best practices during the PPQ stage can prevent a drug approval from stalling out on the final lap.

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Pharmacologic approaches to treating aging are edging closer to maturity
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New treatments offer the promise of tackling age-related disease multimorbidity
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Novel therapeutic approaches to aging are creating a healthspan market with staying power

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