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HYBRID STERILISATION

The next steps in healthcare sterilisation are characterised by hybrid technologies and intelligent systems that combine methods such as plasma, vapour, UV-C light, and gas-based sterilisation to overcome the individual limitations of traditional techniques. The focus is moving towards adaptive sterilisation, smart monitoring systems, material compatibility, and the integration of digital validation tools that ensure complete sterility across increasingly complex healthcare devices and environments.

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Healthcare sterilisation remains the unseen foundation of patient safety. As healthcare systems evolve, new challenges are emerging, with minimally invasive surgical devices, complex materials, and stricter regulatory standards requiring sterilisation methods that are both versatile and sustainable. The next phase of innovation will centre on a hybrid approach that combines the proven effectiveness of established technologies with intelligent control systems, ensuring sterility without compromising materials or the environment.

How Hybrid Sterilisation Is Transforming Healthcare

Hybrid sterilisation represents a major departure from traditional sterilisation models. By combining the strengths of different modalities, such as hydrogen peroxide plasma with UV irradiation or vapour sterilisation enhanced by ozone or low-temperature gas plasma, facilities can achieve higher efficacy while maintaining material integrity. This is particularly vital for advanced polymers, bioresorbable implants, and complex medical instruments that cannot tolerate high heat or humidity.

At the same time, healthcare providers and sterilisation professionals are increasingly implementing digital traceability systems, real-time monitoring, and data-driven validation to improve reliability and compliance. These innovations shorten turnaround times for sterilised instruments, enhance workflow efficiency, and reduce overall treatment time.

Low-maintenance, modular sterilisation units, AI-assisted cycle optimisation, and cloud-connected data environments enable hospitals and contract sterilisation providers to manage multiple sterilisation processes remotely and securely. Open-source data platforms also promote collaboration between healthcare institutions, equipment manufacturers, and regulators, creating the foundation for interoperable sterilisation ecosystems.

The New Era of Sterilisation Innovations

This new era is defined not only by technology but also by collaboration and adaptability. In hybrid sterilisation facilities, robots and automated conveyors transfer sterile loads seamlessly between processes, while human operators concentrate on quality control and validation. Digital twins of sterilisation chambers and processing lines enable engineers to simulate and optimise cycles before implementation, reducing costs and environmental impacts.

However, progress also brings challenges. Cybersecurity is now a top priority for sterilisation networks that handle sensitive patient and device data. Regulatory agencies are introducing stricter digital validation standards, while sustainability requirements are accelerating the move away from single-use materials and energy-intensive sterilisation systems. The balance between innovation, compliance, and environmental responsibility is increasingly influencing strategic decisions across the industry.

The Sterilisation Summit Europe 2026 will explore this transformation in depth, from the science behind hybrid sterilisation to the business models, regulatory frameworks, and digital tools that will shape the future of healthcare sterilisation. The event will bring together healthcare providers, sterilisation experts, equipment manufacturers, regulatory authorities, and policymakers for a global dialogue focused on ensuring sterility, safety, and sustainability within an increasingly complex healthcare environment.

This is the moment to redefine sterilisation as an intelligent, interconnected process that safeguards patients, supports innovation, and advances the healthcare systems of tomorrow.

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Topics on the agenda

THE ROLE OF NANOPARTICLES IN ENHANCING STERILISATION EFFICACY FOR MEDICAL DEVICES

Day 1: undefined

11:30 - 11:55

STERILISATION VALIDATION: IMPORTANCE OF A FULLY VALIDATED IFU

Day 1: undefined

15:30 - 15:55

FAILURE INVESTIGATION FOR ROUTINE /STERILIZATION REVALIDATION FAILURE

Day 2: undefined

10:10 - 10:35

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