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Cleaning and Bio-cleaning

Cleaning Validation Strategy / Optimization of Best Practices and Cleaning Cycles / Visual Inspection Control

When?

December 02 & 03, 2025

Where?

Lyon, France

Format?

Conferences, Partner Sessions & Exhibition

Introduction

Master every step of your cleaning and disinfection strategies: from design to digitization.
Take part in two days of in-depth discussions to strengthen your skills. This comprehensive program, combining theory and industrial feedback, is designed to give you the tools you need to optimize your processes.
• Prevent risks at source: From the outset, you will explore the principles of hygienic design for premises and equipment. Lectures will use concrete examples to illustrate how design flaws can lead to contamination and how to avoid them through best practices.
• Build a robust validation strategy: Learn how to precisely define your acceptance criteria and your worst-case approach. A key session will guide you in implementing a validation strategy for indirect contact surfaces (such as vibrating bowls, caps, or isolators), in accordance with the strict requirements of Annex 1. A practical case study will even be dedicated to the validation of isolator cleaning in non-sterile powdery areas.
• Optimize your daily operations: Reinforce your best practices, whether by choosing the right types of fabrics to avoid contamination or by effectively managing Class A/B inputs. A comparative session will analyze the advantages of manual methods versus automated approaches, such as the use of UV.
• Mastering the regulatory challenges of disinfectants: A conference will address the selection of disinfectants for clean rooms and, crucially, the management of post-application residues. You will discover mitigation strategies, such as mechanical action or rinsing.
• Putting people and performance at the heart of the process: Visual inspection remains a critical step. You will discover the best methods for empowering and mastering this skill within your teams.
• Looking to the future: the digitization of cleaning processes and a strategy for continuous monitoring of your processes for premises and equipment are essential approaches to ensuring sustainable performance.
Join us for two days of conferences, workshops, and networking to transform your cleaning challenges into opportunities for operational excellence.

PROGRAM

Related articles

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La Vague 85 / Avril 2025
Many sterile pharmaceutical production sites are upgrading their equipment to provide greater containment and safety, particularly in aseptic filling lines. Eliminating direct human intervention in critical areas is central to the contamination control strategy. This trend is accelerating with the new version of Annex I of the European GMPs. Indeed, from point 2. Principle (i.) it is clear that “the use of appropriate technologies (e.g., restricted access barrier systems (RABS), [...]) should be considered to increase product protection [...]”.

Managing the performance of cleaning validations: a major industrial challenge.

La Vague 65 / Avril 2020
Can we talk about performance in cleaning validation exercises? How can it be measured? These exercises are known to be “time-consuming,” as indicated in Appendix 15 of the GMP, and therefore often costly to implement. Defining and measuring this performance enables the cleaning validation process to be improved and makes it easier for manufacturers to apply. It is therefore essential to be able to control it.

Validation of cleaning processes: why and how to validate the associated analytical and sampling methods.

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