Upcoming Webinar: Prevent Failure by Designing your Cleanroom Monitoring System to meet cGMP

Upcoming Webinar: Prevent Failure by Designing your Cleanroom Monitoring System to meet cGMP Medium Image
In this webinar, Jason Kelly, VP of Services will cover the implementation of a Monitoring System (EMS) in the framework of cGMP.
Learn how to initiate an EMS project from start to finish, beginning with a Risk Assessment and completing with a Performance Qualification.  You will also learn how to set up Service Level Agreements to ensure your business continuity remains paramount and downtimes are kept to a minimum. 
By partnering with the right EMS vendor, you can leverage the best expertise to ensure your EMS project, and just as importantly your EMS environmental data, is meaningful and that data is secure and accurate. 
Understand how to get the most out of your EMS and the data it produces, as well as how to follow an EMS process flow to Supercharge your Contamination Control Strategy.
Register today to secure your seat!
For the North America Webinar:
10:00 AM - 11:00 AM / Wednesday, August 26, 2020 (PDT), 
45 Minute Webinar / 15 Minute Q&A 
For the International Webinar:
9:00 AM - 10:00 AM / Wednesday, August 26, 2020 (GMT), 
45 Minute Webinar / 15 Minute Q&A
To register, click  HERE.
 All attendees questions will be addressed during the webinar Q&A and after by direct email.
*** Webinar Overview ***
During this webinar, we will cover:
* Risk Based approach to EMS design
* What is GMP?
* URS importance and Traceability Matrices
* What sensors connect to an EMS?
* How do particle counters detect contamination?
* The sizes of particles in your cleanroom
* ISO 21501 and particle counter accuracy
* EMS overview and redundancy
* EMS software interface
* EMS Process Flow - EMS design and Implementation
* 21CFR11 testing and compliance
Who Should Attend?
  • You need to gain information on implementing an EMS for your company
  • You need to develop a Contamination Control Strategy for aseptic manufacturing
  • You are responsible for EMS data and report generation for batch release
  • You perform QA of EMS data
  • You are responsible for supervising product manufacturing
  • You are part of Environmental Monitoring Plan execution team
  • You are part of Validation Master Plan team
  • You are a cleanroom consultant
  • You want to meet GMP for cleanroom monitoring
Be Sure to Reserve Your Spot!