How CDMOs With In-House Analytical Capabilities Save Sponsors Risk, Cost, and Time

by 3PBIOVIAN

Analytical services are critical to the development and manufacture of safe and effective biopharmaceuticals. These analytical services often are outsourced to third-party laboratories, and in some ca...

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Project Management in Biologics Development: Keys to Successful CDMO Collaboration

by 53Biologics

Biologics development is complex. Each project involves multiple stakeholders, tight timelines and strict regulatory standards. For companies working with a Contract Development and Manufacturing Orga...

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Alzheimer’s Disease Clinical Trials and Emerging Therapies: Transforming Patient Care Through Innovation

by Pivotal

Alzheimer’s disease (AD) is one of the most significant and pressing challenges in modern healthcare. Affecting more than 50 million people worldwide1, AD places an immense and growing social and ec...

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53Biologics, galardonada con el premio pyme del año 2025 de Valladolid

by 53Biologics

53Biologics ha sido distinguida hoy con el Premio Pyme del Año 2025 de Valladolid, un reconocimiento otorgado por Banco Santander y la Cámara de Comercio de Valladolid, en colaboración con la Cáma...

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Preclinical Contract Research to Accelerate Drug Development: Study Design and FDA Toxicology Guidelines Considerations

by AMSbiopharma

This article explores the scope of preclinical contract research, best practices in study design, key FDA toxicology guidelines for compliance, and common challenges that impact project efficiency.

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3PBIOVIAN Drives a Pioneering Project with the Navarre Ecosystem to Improve the Efficacy and Accessibility of CAR-T Therapies

by 3PBIOVIAN

A consortium formed by the Clínica Universidad de Navarra, the Hospital Universitario de Navarra, the University of Navarra, the research centers FIMA and Navarrabiomed, and the technology companies ...

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Joan Puig – CEO at Kymos Group

by GENESIS Biomed

Joan Puig: “In inorganic growth in Europe, cultural difference is one of the most important challenges”.

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Superando las barreras al reclutamiento de pacientes: soluciones para las barreras más comunes

by Sermes CRO

El reclutamiento de pacientes sigue siendo uno de los mayores retos en la ejecución de ensayos clínicos. No es extraño que más del 80% de los estudios se retrasen por dificultades para alcanzar lo...

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The EHDS in clinical research: what changes for CROs and sponsors (and how to prepare)

by Sermes CRO

The European Health Data Space (EHDS) will transform the way health data are identified, requested, and used in clinical research, pharmacovigilance, health technology assessment, and regulatory activ...

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3PBIOVIAN and Universidad CEU San Pablo formalize an alliance to promote the development of new professionals in health biotechnology

by 3PBIOVIAN

3PBIOVIAN, a company specialized in the development and manufacturing of biological medicines for third parties, and Universidad CEU San Pablo in Madrid have signed a Business Collaboration Agreement ...

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The Ethical Challenges of Advanced Therapies: A Necessary Reflection

by Sermes CRO

Advanced therapies, encompassing gene treatments, cell-based therapies, and tissue-engineered products, have marked a turning point in modern medicine. These innovations offer solutions for severe dis...

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BioIVT acquires BeCytes Biotechnologies to boost preclinical research in Europe

by Parc Científic de Barcelona

The U.S. multinational BioIVT, a global leader in the development of high-quality biological samples and research services for drug and diagnostic development, has acquired the Catalan company BeCytes...

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