Cambrex Industry Insights
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The Delicate Dance: When Phase-Appropriate Decisions Carry More Risk
9/23/2026
Early drug development demands speed, but some decisions carry long-term consequences. Learn which process and analytical choices require teams to look beyond the next milestone.
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Outsourcing Stability Storage: A Cost-Effective And Quality-Driven Approach
8/22/2024
Partnering with a leader in outsourced stability storage is revolutionizing the pharmaceutical and medical device industry by saving costs and resources, and ensuring product quality and compliance.
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Nitrosamine Analysis: Solutions For Risk Management And Analytical Testing
8/22/2024
Testing for nitrosamines is essential in the development and manufacturing of Active Pharmaceutical Ingredients (APIs) and drug products to ensure safety and compliance.
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Continuous Manufacturing: An Evolving Technology For Drug Manufacturing
8/21/2024
Explore the exciting developments in continuous manufacturing and learn how leveraging this innovative technology can help improve manufacturing processes and discover new clinical candidates.
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Extractables And Leachables: Risk Management And Analytical Solutions
10/11/2023
Partnering with a CDMO that offers comprehensive and robust E&L studies can help facilitate a smooth product launch by ensuring minimal impact from impurities, all while mitigating risks.
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How Life Science Is Reshaping Supply Chains In Response To COVID-19
1/24/2022
COVID-19 disruptions led companies to rethink global supply and outsourcing strategies. A survey of 117 biopharma leaders gauged how that experience is shaping attitudes toward resilience.
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Digital Transformation In Regulatory: Achieving Excellence Virtually
1/24/2022
As the industry looks forward, key decisionmakers in pharma and biotech companies were surveyed to assess their views on undertaking regulatory processes virtually.
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Balancing Cost Efficiencies In The Drug Development Process
1/24/2022
Cost efficiencies and expertise again go hand in hand, with companies often outsourcing or partnering primarily to gain access to manufacturing know-how.
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Assessing End-To-End Drug Development Partnerships
1/24/2022
As drug development becomes increasingly expensive and complex, pharma companies are relying on CDMOs to maximize efficiencies. Examine the opportunities and challenges of end-to-end arrangements.
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Addressing Development And Manufacturing Upheaval
1/24/2022
Growing complexity and risks in drug development and supply have implications for outsourcing models. See how to structure and manage CDMO partnerships for a future with uncertainty and disruption.