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November 16 - November 18

Virtually or in Dublin, Ireland

Design a Cleaning Program that Impresses Regulatory Investigators


A compliant cleaning validation program is essential for a successful regulatory inspection. Even today, many have struggled to develop effective processes and keep up with evolving sterile regulations that meet an inspector’s expectations. This conference is designed for those professionals in charge of developing, implementing and maintaining new or legacy cleaning validation programs. Attend this conference and walk away with the innovative processes, techniques and tools that have an immediate impact for your company and professional development.


Top 10 Reasons to Attend:

  1. Overcome the Top Five Cleaning Validation Challenges
  2. Understand EU Annex 1 Revisions – Your Guide to Sterile Manufacturing
  3. Implement a Risk-Based Cleaning Validation – Key Elements to a Successful Program
  4. Establish Acceptance Criteria and Health-Based Limits in Cleaning Validation
  5. Create Best-in-Class Cleaning Validation Documents – Master Plans, SOPs, Assessments, Technical Reports and More
  6. Develop Cleanroom Validation, Disinfection and Environmental Monitoring Procedures
  7. Manage Changes in Cleaning Validation Processes
  8. Use Advanced Analytical Methods for Cleaning Validation
  9. Set Critical Cleaning Process Parameters and Critical Quality Attributes
  10. Qualify Water Systems, Clean Steam Systems and Process Gasses


Personnel in the Following Environments Should Attend:

  • Validation
  • QA/QC
  • Engineering
  • Regulatory Affairs
  • Compliance
  • Manufacturing
  • Laboratory


This event is also appropriate for business development and sales managers that offer innovative solutions for quality, validation and engineering professionals in the life science environment.



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  • Fundamentally we exist for one reason: To accelerate our clients’ path to success. Our approach is simple; we put the client’s interests first. We don’t stop until it’s right. And we’ll do whatever it takes to get there.
    Website: https://commissioningagents.com

  • Since 1949, Ellab is a leading manufacturer of a full line of wireless, real-time data loggers and wired thermocouple validation systems with temperature, humidity, pressure, vacuum, conductivity and CO2 sensor options. Additionally, Ellab offers temperature standards, calibration dry blocks and liquid baths, custom fittings, accessories, and thermocouples. We also offer on-site qualification, validation and calibration services for thermal validation processes ranging from -196°C to 400°C. Typical environments often include -80°C freezers, incubators, stability chambers, autoclaves, and ovens.
    Website: https://www.ellab.com/

  • Novatek International provides a new breed of all-encompassing, process-driven LIMS and other software solutions that target the pharmaceutical, biotech and other health-care industries. Our unique portfolio of out-of-the-box, easy to use software solutions features specialized modules that help you manage all aspects of your quality environment with less effort and time. Novatek delivers solutions that go beyond LIMS for total enterprise wide automation.
    Website: https://ntint.com/


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November 16
November 18
Event Category:


Virtually or in Dublin
Virtually or in Dublin, Ireland + Google Map

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