Remove topic contract-manufacturing-biopharmaceutical-production
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Genenta Science signs manufacturing service deal with AGC Biologics

Pharmaceutical Technology

Genenta Science and AGC Biologics have signed a development and manufacturing service agreement (MSA). Under the deal, AGC Biologics will be responsible for manufacturing the cell therapy lentivirus-based product for the ongoing clinical programmes of Genenta Science.

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AGC and RoosterBio partner for cell and exosome therapy manufacturing

Pharmaceutical Technology

Biopharmaceutical contract development and manufacturing organisation (CDMO) AGC Biologics has entered a strategic collaboration with RoosterBio to expedite the manufacturing of cell and exosome therapies. It will also have the potential to scale to Phase III clinical development and commercial manufacturing.

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Exploring the gene therapy biomanufacturing landscape

European Pharmaceutical Review

Ahead of her presentation on the future of biomanufacturing at CPHI Barcelona, Sheila Ann Mikhail, the co-founder and former CEO of AskBio, engages in a conversation about gene therapy, artificial intelligence, and the importance of being a well-informed innovator when selecting a manufacturing partner.

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Rentschler Biopharma and Ikarovec partner to expedite new gene therapies

Pharmaceutical Technology

As we look to find new and better ways to treat ophthalmic diseases, we want to get it right and ensure that our product candidates can be scaled up appropriately for each development stage and, ultimately, for commercialisation. The company is a global contract development and manufacturing organisation (CDMO) for biopharmaceuticals.

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CPHI Barcelona 2023 – Event preview

European Pharmaceutical Review

It provides unparalleled opportunities to source valuable partnerships, secure contracts, and stay ahead in a rapidly evolving industry. Attendees can plan meetings, bookmark interesting exhibitions and products, and receive personalised recommendations from AI regarding products, exhibitions and relevant content sessions.

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Pharmaceutical microbiology: key developments 2022

European Pharmaceutical Review

This Q&A covers the key developments in pharmaceutical microbiology in 2022, featuring insight from pharmaceutical microbiology experts: Dr Tim Sandle, Head of Microbiology, Bio Products Laboratory Limited. He questioned how regulators will enforce revisions to Good Manufacturing Practice (GMP) regulations.

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‘Right shoring’ API production in Europe

Pharmaceutical Technology

In the 1990s, generic pharmaceutical companies in the European Union (EU) offshored the manufacturing of active pharmaceutical ingredients (API) primarily to China. Despite having large biopharmaceutical companies on home ground, the UK and France experienced major shortages and supply chain issues.