The search for safer, more effective medicines increasingly depends on understanding how biological systems respond to disease, genetic variation, and therapeutic interventions at the molecular level....
Read moreWhen companies evaluate GMP recombinant protein manufacturing, discussions often revolve around timelines, batch size or price per gram.
Read moreMaking the transition from a laboratory-validated test to the industrial manufacture of rapid tests is one of the most critical stages in the life cycle of an in vitro diagnostic (IVD) product.
Read morePurification is often where development programs stall: inadequate method design, suboptimal column selection, or a poor understanding of critical impurity profiles can consume months of development t...
Read moreSterility testing is a core analytical competence at 3PBIOVIAN, with nearly three decades of experience analysing a wide range of product types, including protein‑based and viral products.
Read moreThe way a clinical trial is communicated to patients determines its viability from the very outset. Before assessing inclusion criteria or protocol complexity, patients need to understand what is bein...
Read moreClinical trials in the Intensive Care Units (ICUs) are among the most complex and demanding studies in clinical research. The scientific rationale for studying interventions in critically ill patients...
Read moreIn the day-to-day conduct of clinical trials, one of the factors that most strongly affects patient recruitment and retention is not the scientific design of the protocol, but rather the indirect fina...
Read morePartnership during the last 8 years leverages VIVEbiotech’s decade of experience manufacturing GMP ex- and in- vivo lentiviral vectors for the advanced therapies sector
Read moreTransfection-free stable producer cell line (SCL) offers easy scalability, reduction of cost of goods (COGs), improve vector quality, and low batch variability.
Read moreManaging a clinical trial with a limited population requires rethinking many of the usual assumptions of clinical research. When the number of potential patients is small, every methodological, operat...
Read moreNow advancing 15 next-generation in vivo therapies through high-performance, scalable lentiviral vector manufacturing capabilities
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