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Formulation and filling may be the final step in drug development, but its impact on product success is anything but final. Explore the critical final step in drug development and discover expert strategies that can help streamline operations, reduce risk, and enhance efficiency.
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Efficient fill and finish operations are critical to the success of cell and gene therapies, where maintaining sterility and regulatory compliance can be especially challenging. Discover end-to-end solutions that streamline fill and finish operations for cell and gene therapies, as well as learn how single-use systems help ensure sterility and compliance.
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As regulatory expectations evolve, manufacturers are under increasing pressure to ensure aseptic processes meet the latest standards. Learn how single-use technologies help reduce contamination risks and support compliance with updated EU GMP Annex 1 guidelines for aseptic processing and sterile drug manufacturing.
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As regulatory expectations grow more stringent, biomanufacturers are rethinking their fill-finish strategies to stay ahead. Uncover how biomanufacturers are adopting single-use tech to boost compliance, reduce labor, and streamline fill-finish operations from the ground up.
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