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Virtual QC Microbiology Training

 
 

QC Microbiology Training
has gone Virtual.

Register Here

Due to the current Covid - 19 situation, we will continue to offer our virtual training sessions in 2022.

We invite you to join us for our QC Microbiology Virtual Training.

In this 2-day course, we’ll be covering the 4 most critical tests performed by
Pharma Industry QC Microbiology laboratories.

  • Bioburden
  • Environmental Monitoring
  • Pyrogens (MAT)
  • Sterility Testing

Participants may attend all or individual sessions as applicable:

Cost:

$250 per individual session $800 for all sessions

Participants may attend all four or choose individual sessions. Group discounts are available.
To register, click here.

Remote Learning Dates

February 22 – 23, 2022

November 15 – 16, 2022

Each module consists of approximately half a day of training.


Remote Sessions: February 22 - 23, 2022*

Day and Time:

February 22, 2022 February 23, 2022

Bioburden
1:00 pm - 3:00 pm (EST)

Sterility
3:30 pm - 5:30 pm (EST)

Pyrogen Testing
1:00 pm - 3:00 pm (EST)

Environmental Monitoring
3:30 pm - 5:30 pm (EST)


Remote Sessions: November 15 - 16, 2022*

Day and Time:

November 15, 2022 November 16, 2022

Bioburden
1:00 pm - 3:00 pm (EST)

Sterility
3:30 pm - 5:30 pm (EST)

Pyrogen Testing
1:00 pm - 3:00 pm (EST)

Environmental Monitoring
3:30 pm - 5:30 pm (EST)


Register

Who should attend this QC Training Session?

The course is designed for quality control microbiology professionals, quality assurance or regulatory affairs personnel who have responsibility for the performance of Bioburden, Sterility, Environmental Monitoring, & Pyrogen (MAT) testing or for data review, as well as pharmacists performing sterile compounding.

What will you be able to accomplish after attending this course?

  • Understand the current requirements of pharmacopoeias and be familiar with good testing procedures from method development / validation through to routine test result interpretation
  • Take preventive actions to avoid false positive or false negative test results
  •  Develop and optimize testing procedures
  • Understand and identify root causes for common issues

*Registration accepted for attendees located in the US/Canada and Puerto Rico