European Pharmaceutical Review

Enhancing manufacturing with process analytical technology (PAT) in 2025

During this virtual panel, industry experts will explore the latest developments and biggest challenges in process analytical technology (PAT) today.

webinar

Applying ISO/TR 14644-21 – Airborne particle sampling techniques

Watch this webinar as GMP expert Mark Hallworth discusses the difference between cleanroom classification and monitoring of the new ISO 14644 Technical Report 21 focuses in section 4.0 and 5.2.

Editor's Spotlight

Podcast 24 – Developing modifier gene therapy for Ocular diseases

podcasts

EPR Podcast 24 – Developing modifier gene therapy – Ocugen

Biologic could reduce treatment burden for children with haemophilia A

By Catherine Eckford (European Pharmaceutical Review)

Unlocking intellectual property potential in European pharma

By Joshua Harris (Burford Capital)

Draft regulatory guidance on personalised cancer therapies published

By Catherine Eckford (European Pharmaceutical Review)

Moderna reports record for UK clinical trials in 2023/24

By Catherine Eckford (European Pharmaceutical Review)

Latest Pharma Industry News

news

Novartis nets potential first-in-class medicine in new cardiovascular acquisition

The potentially multi-billion-dollar deal strengths Novartis’ late-stage pipeline for cardiovascular therapies, signalling advancement of novel treatments for heart disease.

news

By Joshua Harris (Burford Capital)

article

Harnessing industry advancements to accelerate upstream process development

Here, Shidong Shi, Head of Upstream Process Development, and Li Yang, Vice President of CMC Development at Altruist Biologics, discuss…

By Dr Li Yang (Altruist Biologics), Dr Shidong Shi (Altruist…

article

Biosimilar medicines: the intersection of access, affordability, and innovation

In this article, Julie Maréchal-Jamil, Director, Biosimilar Policy & Science, Medicines for Europe, explores the strategies needed at European and…

By Julie Maréchal-Jamil (Medicines for Europe)

Image depicting technology transfer for biologics upstream processing

article

Considerations for a successful tech transfer of a biologics upstream…

Bioprocess experts from Lonza discuss how molecular format and the product lifecycle phase impact the process, risks and outcomes of…

By Maolong Liu (Lonza Biologics), Neil Judd (Lonza), Nikki Nogal…

pharma dealmaking M&A mergers and acquisitions

article

M&A outlook for pharma in 2025

For a strong 2025, dealmaking should be central to the life sciences strategy, says EY’s annual M&A report.

By Catherine Eckford (European Pharmaceutical Review)

article

Transitioning to digital product information to ensure a sustainable future

Sarah Moores, Global Sustainability Director at AstraZeneca, discusses the potential scope for establishing electronic product information (ePI) in the pharmaceutical…

By Sarah Moores (AstraZeneca)

Latest from our partners

webinar

Monocyte activation test (MAT): Insight into examining regulations and markets…

Watch this webinar to learn about the current regulations on the monocyte activation test (MAT) and the new type of…

Whitepapers/App Notes/Posters

Regulatory Authority Inspection Comparison

A guide on what to expect during a regulatory inspection and the differences in the approach taken by three of…

Video

On-demand webinar: High speed for your material analysis

In this webinar, discover how an innovative 2-in-1 method for material analysis accelerates visual and chemical particle analysis in the…

Event

PharmaLab Congress 2025

The 2025 PharmaLab Congress offers a diverse programme with insights on the latest advances in analytical and microbiological quality control…

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