Metabolomics and lipidomics in drug discovery and development: analytical approaches for biomarker discovery and preclinical research

by AMSbiopharma

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....

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Recombinant Protein Production Under GMP: Key Decisions That Define Success

by 53Biologics

When companies evaluate GMP recombinant protein manufacturing, discussions often revolve around timelines, batch size or price per gram.

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IVD contract manufacturing: scaling up rapid tests without risk

by OPERON

Making 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.

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Peptide purification in drug development: methods, techniques, and analytical strategies

by AMSbiopharma

Purification 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...

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3PBIOVIAN Strengthens its Sterility Testing Capabilities

by 3PBIOVIAN

Sterility 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.

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Patient‑centred materials design: impact on recruitment and adherence

by Sermes CRO

The 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...

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Clinical Trials in an Intensive Care Unit: Challenges and Successful Implementation

by Pivotal

Clinical 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...

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Impact of financial compensation on patient recruitment and retention in clinical trials

by Sermes CRO

In 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...

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VIVEbiotech and Zelluna Partnership to Advance Off-the-Shelf TCR-NK Cell Therapy with GMP Lentiviral Vectors

by VIVEbiotech

Partnership during the last 8 years leverages VIVEbiotech’s decade of experience manufacturing GMP ex- and in- vivo lentiviral vectors for the advanced therapies sector

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VIVEbiotech Expands Lentiviral Vector Manufacturing Capabilities with EvoLVcell

by VIVEbiotech

Transfection-free stable producer cell line (SCL) offers easy scalability, reduction of cost of goods (COGs), improve vector quality, and low batch variability.

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How to Manage Trials in Small Populations: Lessons from Rare Diseases

by Sermes CRO

Managing 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...

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VIVEbiotech adds newest in vivo lentiviral vector-based therapeutic programs

by VIVEbiotech

Now advancing 15 next-generation in vivo therapies through high-performance, scalable lentiviral vector manufacturing capabilities

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