CPHI Milan 2
CPHI Milan newsletter
PCI High Potent Manufacturing
LB Bohle – 10.06.2025
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Current Edition

Current Edition

Subsection - CDMO

Examining how innovative technologies, integrated manufacturing approaches and AI are shaping manufacturing.

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Subsection - Injectables

Exploring advances in injectable drug delivery and sterile manufacturing, designed to improve patient-centric delivery.

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Subsection - Neurodegenerative Diseases

Exploring emerging approaches to neurodegenerative disease research and treatment.

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Subsection - Nasal & Pulmonary

Highlighting how advances in nasal and pulmonary drug delivery, formulation, devices and analytics are enabling more complex therapies.

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CPHI 2027
DDL 2026

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Nipro August 26

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Merxin March 2026

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Aurisco 300×250

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Lifecore Biomedical
Editorial Archive

Evolving Quality Risk Management: A Deep Dive into ICH Q9 (R1) with Kevin O’Donnell (HPRA) on the Pharma Conversations Podcast

In a recent episode of the Pharma Conversations podcast, Kevin O’Donnell of the Health Products Regulatory Authority (HPRA) offered a detailed and thought-provoking ...
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Editorial Archive

Solstice Advanced Materials on Powering the Global Shift to Low-GWP Inhaler Propellants

Solstice Advanced Materials outlines its perspective on the transition to lowGWP propellants in an interview with International Pharmaceutical Industry Journal, ...
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Editorial Archive

Terumo Pharmaceutical Solutions on Integrated CDMO Services

International Pharmaceutical Industry Journal speaks with Michele Guasti, Global Product Manager at Terumo Pharmaceutical Solutions Division. The discussion explores...
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Editorial Archive

PFAS and Pharmaceuticals: Why the Industry Can No Longer Afford to Wait

Few regulatory issues have the potential to reshape pharmaceutical manufacturing as profoundly as PFAS. Often referred to as "forever chemicals", per- and polyfluoro...
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Editorial Archive

Differences Between US and EU Pre- and Post-Market Regulatory Obligations

Typically, global companies developing innovative therapies are familiar with the differences between regulatory systems in the United States and European Union. In ...
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Editorial Archive

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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Editorial Archive

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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Editorial Archive

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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Editorial Archive

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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Editorial Archive

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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MedPharm 16/07

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Biopharma group march 2026

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Silgan March 2026

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Terumo 06/26

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Scott Pharma – 25.03.2025

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Bespak

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Solstice

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