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Two researchers in a GMP compliant cleanroom operate manufacturing equipment
The collaboration combines mRNA sequence optimization with end-to-end GMP manufacturing to support streamlined development and clinical-scale production.
Nov. 7, 2025
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The partnership will combine Mabqi’s antibody discovery capabilities with Abzena’s development and manufacturing services to streamline workflows.
Nov. 7, 2025
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The company plans to open new facilities in Ohio and California and expand operations in Alabama to strengthen supply chain resilience.
Nov. 6, 2025
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Evotec company logo displayed on mobile phone
The completed deal expands Sandoz’s biosimilar manufacturing footprint while enabling Evotec to transition toward a more asset-light, technology-driven business model.
Nov. 6, 2025

Learning Resources

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Advancements in cleanroom technology are redefining pharmaceutical manufacturing with energy-efficient HVAC, sustainable materials, and intelligent airflow. However, much more...
Oct. 28, 2025
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Explore proven alternatives to fetal bovine serum (FBS). Discover how donor bovine serum and other options can reduce cost and supply risks while maintaining performance in bioproductio...
Oct. 21, 2025
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Join industry specialists as they share their insights, experiences, and strategies to enhance efficiency, reduce costs, and improve product quality in the production of non-traditional...
Nov. 11, 2025
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Innovative approaches to help address high productive methods of mAb polishing
Sept. 24, 2025

Podcast

Editors' (re)View

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While Big Pharma has the resources to invest in domestic production, smaller biotech companies increasingly rely on contract manufacturers who need help.
Nov. 7, 2025
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The two bellwethers of the CDMO industry reported strong financial results for the third quarter of 2025 amid uncertainty in geopolitics and funding.
Oct. 24, 2025
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While the plant was recently hit with the FDA’s most severe post-inspection classification, it is a facility that has been plagued with problems for several years.
Oct. 17, 2025
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Industry stakeholders who attended the annual Cell & Gene Meeting on the Mesa this week in Phoenix emphasized the positive, despite formidable challenges.
Oct. 10, 2025

Production

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Panelists at the 2025 Cell & Gene Meeting on the Mesa laid out the challenges and opportunities facing the industry as it looks to produce these therapies at scale.
Oct. 7, 2025
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In the fast-changing pharmaceutical sector, packaging is more critical than ever to patient safety and product provenance.
Oct. 1, 2025
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Despite industry setbacks with adeno associated virus-based gene therapy programs, the issue is “largely overblown” for Repligen, contend Leerink Partners analysts.
Sept. 11, 2025
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The CDMO acquired the 128,000-square-foot cell and gene therapy facility in Hopewell last year, which is now ProBio’s North American hub.
Aug. 25, 2025

Development

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The agency is reviewing clinical trials that involve sending U.S. patients’ living cells to China and other “hostile countries” for genetic engineering and return infusion.
Sept. 22, 2025
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With manufacturers under increasing pressure to reduce costs, enhance compliance, and accelerate production timelines for high quality drugs, they are increasing their investments...
Aug. 25, 2025
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The future of non-clinical research may depend on integrating VCGs for a more humane and efficient approach.
Dec. 5, 2024
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Improve bioreactor performance, accelerate process development from benchtop to production, assess respiratory efficiency with continuous CO2 monitoring, eliminate potential interferenc...
Nov. 22, 2024

Information Technology

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Software platforms can seamlessly integrate with emerging technologies to unlock efficiencies, strengthen sustainability and enable proactive prevention of disruptions.
Sept. 10, 2025
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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...
March 5, 2025
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Discover the latest contract manufacturing key trends for the life science industry, including compliance, digital transformation and more. Don't let your organization fall behind...
Feb. 24, 2025
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As the life sciences sector evolves with personalized medicine, biologics, and digitalization, manufacturers must innovate, invest in advanced tech, and adopt agile manufacturing...
Jan. 30, 2025

Compliance

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Marc Casper contends Thermo Fisher’s pharma and biotech customers will be able to navigate the Trump administration’s MFN drug pricing framework and tariffs.
Oct. 22, 2025
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This episode of Off Script: A Pharma Manufacturing Podcast features a conversation with Jana Falkenberg, senior legal counsel and corporate compliance officer at Vetter Pharma...
Oct. 17, 2025
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CEO Pascal Soriot announced the deal with President Trump on Friday, noting that it includes a three-year exemption from U.S. tariffs for AstraZeneca’s products.
Oct. 10, 2025
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Designed for the review of abbreviated new drug applications, the program is meant to strengthen the domestic pharmaceutical supply chain in the United States.
Oct. 6, 2025

Quality & Risk

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Cytiva’s 2025 Global Biopharma Index shows widening gaps across regions as talent shortages, regulatory strain, and uneven sustainability progress weigh on growth.
Oct. 27, 2025
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According to US Pharmacopeia, 58% of KSMs used for U.S.-approved active pharmaceutical ingredients are sole sourced from a single country.
Oct. 20, 2025
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The industry’s inability to make products efficiently and at scale is due to the complexity of the supply chain, panelists said at the Cell & Gene Meeting on the Mesa.
Oct. 8, 2025
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Read more about how WarmMark QR addresses today’s common cold chain monitoring challenges through an innovative combination of visual and digital tracking.
April 25, 2025