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Home > Resources > Whitepapers > WHO considerations on Regulatory Convergence of Cell and Gene Therapy Products
December 16, 2021
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MaxCyte is a leading commercial cell-engineering company focused on providing enabling platform technologies to advance innovative cell-based research as well as next-generation cell therapeutic discovery,
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Filamentous fungi of the phylum Basidiomycota are considered as an attractive source for the biotech‑ nological production of composite materials. The ability of many basidiomycetes to accept residual lignocellulosic plant biomass from agriculture and forestry.
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Imaweld® is thermoplastic elastomer tubing particularly designed to transfer critical fluid in pharmaceutical and biopharmaceutical applications.
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Biotechnology and pharmaceutical industries continue to experience increased pressure on financial performance due to several factors.
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Regulatory teams at life science companies are finding that effective regulatory information management (RIM) has become critical to their operations.
whitePaper | June 23, 2022
Cell and gene therapies require both efficient and reliable freeze-thaw systems. Building the most effective system depends on selecting the right materials and instruments.
whitePaper | April 16, 2020
Accurate diagnosis is the cornerstone of medicine; it is essential for informed care and promoting patient and family well-being. However, families with a rare genetic disease (RGD) often spend more than five years on a diagnostic odyssey of specialist visits and invasive testing that is lengthy, costly, and often futile, as 50% of patients do not receive a molecular diagnosis.
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