On Demand

Environmental Cleanroom Monitoring for Pharma 4.0.

This webinar describes the basic concept of a dedicated pharmaceutical cleanroom monitoring system (FMS) in comparison with other multi-application systems such as Building Management Systems (BMS), with clear pros and cons.

Differences between computer-based and industrial designed FMS will be discussed, with a focus on system reliability and data integrity aspects.

Additionally, pharmaceutical users will get a “knowledge toolkit” to ensure technical, regulatory, and quality requirements insights to ensure a proper facility monitoring system design, maximize ROI and ensure regulatory acceptance.

In this webinar you’ll learn:

  • The main differences between a dedicated cleanroom FMS and BMS;
  • The must-have design to be ready for the digital transformation
  • What to expect from regulatory changes and pharmaceutical industry trends
Webinar Presented By:
Daniele Pandolfi
Global Product Line Manager, Software, Systems and Services Particle Measuring Systems

With over 17 years of experience in contamination control, Daniele Pandolfi excels in product management, collaborating with teams worldwide and staying up to date with industry regulations and trends.

He is a seasoned public speaker at events such as ISPE, PDA, and iInternational pharmaceutical exhibitions. His expertise has been featured in multiple publications including the American Pharmaceutical Review and relevant GMP technology publication for pharmaceutical industry.

With a strategic and innovative approach, Daniele is passionate about sharing knowledge on regulatory requirements, technological trends, and contamination control experiences to help pharma users achieving their compliance goal.