Conference Highlights
Learn More About the 2025 ISPE Annual Meeting & Expo

Biotech Sessions at the 2025 ISPE Europe Annual Conference Highlight ATMPs including Large Molecules and Cell and Gene Therapies
The biotech sector, which includes advanced therapy medicinal products (ATMPs) including large molecules and cell and gene therapies, has been the fastest growing market in the pharmaceutical industry for years and this is not expected to change in the next few decades. In addition to products already on the market and new products in development, the market will additionally grow in biosimilars, biobetters, and combined products such as antibody drug conjugates as well as cell and gene therapies.

A Message from the 2025 ISPE Europe Annual Conference Chair
The 2025 ISPE Europe Annual Conference will take place from Monday, 12 May to Wednesday, 14 May 2025 in London, United Kingdom. Participants will be able to attend in person or virtually. Heather Watson, Director, TenTenTen Consulting Limited, will serve as the 2025 ISPE Europe Annual Conference Chair. Below, Heather shares her personal insights on what attendees can look forward to at the upcoming conference.

Announcing Pharma 4.0™ and Digitalization Transformation Track at the 2025 ISPE Europe Annual Conference in London, United Kingdom
The future of the pharmaceutical industry is being shaped by rapid advancements in digital technologies, automation, and data analytics. As we look ahead to 2025, the concept of Pharma 4.0™ is no longer just an aspirational vision—it is becoming a transformative reality that will redefine how medicines are developed, manufactured, and delivered to patients.

GAMP® at the 2025 ISPE Europe Annual Conference: Where Quality, AI and Compliance Meet
In today’s rapidly evolving pharmaceutical landscape, advancing technologies, shifting regulatory landscapes, and emerging global challenges such as supply chain disruptions, and drug shortages have significantly impacted how we develop, manufacture, and deliver treatments. These factors underscore the critical need for robust validation approaches for computerized systems to safeguard patient safety, ensure data integrity, and maintain product quality.