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2023 PDA Annex 1 Workshop (Charlotte)

Dec 04 2023 - Dec 05 2023 Harris Conference Center, Charlotte, NC Booth 5 https://www.pda.org/global-event-calendar/event-detail/2023-pda-annex-1-workshop-(charlotte)

See our technology experts at the 2023 PDA Annex 1 Workshop (Dec 4-5), being held prior to the PDA Contamination Control Strategy Workshop (Dec 6-7).

We'll be at both workshops to help industry professionals address challenges with implementation of the new August 2023 EU GMP Annex 1 revision. 

Stop by our booth where we’ll be featuring our Annex 1 ready contamination control monitoring instruments that can help you tackle critical industry challenges. We’ll have in-hand our: 

  • BioTrak™ Real-Time Viable Particle Counter (a biofluorescent particle detector) that eliminates aseptic interventions for microbial monitoring. It combines viable particle counting—also called biofluorescent particle counting (BFPC)—with sample capture capability and ISO-compliant total particle counting to offer a complete solution for pharmaceutical environmental monitoring.
  • AeroTrak™+ A100 Portable Particle Counter that are engineered for technicians to easily perform cleanroom classification, monitoring, or simple root-cause analysis. Just press START and you’re ready for measurement. Features include data integrity to meet Annex 1, enhanced communication options, and intuitive GUI. 

Our contamination control monitoring instruments for pharmaceutical manufacturing are designed to be used alone or as part of a complete TSI Facility Monitoring System. Ask our experts who will be at the workshop to learn more. 

Get a Peek Now

  • Watch video to see how the BioTrak Real-Time Viable Particle Counter can keep patients safe while improving manufacturing profitability.
  • Watch video to see how easy it is to use the AeroTrak+ A100 Portable Particle Counter for Annex 1 compliant cleanroom classification testing.
  • See our full suite of aseptic enviromental monitoring instruments.

About the Workshops

The intent of the workshops is to address the challenges and implications of new Annex 1, specifically to provide attendees with a clear understanding of how to navigate and successfully meet the requirements of the revision. PDA, through a standardized approach for workshop topics, is working to ensure that the information delivered to the industry remains consistent and relevant to the current regulatory landscape.