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Why Predictive Analytics are Crucial for Effective EU-HTAR Implementation

The EU’s Health Technology Assessment Regulation (EU-HTAR) aims to introduce more harmonised, efficient and evidencebased assessments of new health technologies. How...
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Rethinking Clinical Trial Design: Making Patient Value Measurable with Net Treatment Benefit

Patient centricity has become one of the most widely shared ambitions in clinical research. The industry increasingly recognises that engaging patients early in deve...
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Skin Modelling in Cosmetic Science: Tools for Evaluation and Innovation

The global skincare market represents a multi-hundred-billion-dollar industry, with continued growth projected over the coming decade. A significant portion of this ...
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Insider Tips for a Right-the-First-Time Tech Transfer

Driven by complex modalities, global supply chains, and strategic partnerships, increased outsourcing makes tech transfer a critical process for both CDMOs and spons...
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After GLP-1: Can the Industry Keep Up with the Peptide Pipeline?

Understandably, much of the last few years – and the rise of peptides – has been completely dominated by one or two products, namely the now ubiquitous GLP-1 drugs f...
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Designing Quality into the Process: Integrating QbD and PAT for Modern Drug Delivery

Pharmaceutical quality is built on the principle that medicines are manufactured to be consistent and released in accordance with defined specifications. And while t...
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