QC Trends and Insights User Group Meetings 2025

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Enhance your understanding of regulatory requirements for GMP environments

If you’re involved with data integrity and security and responsible for meeting regulatory demands for cleanrooms, laboratory or pharmaceutical water, then you’ll want to save a seat at one of our upcoming user group meetings.

We facilitate these meetings specifically for those who are interested in enhancing their understanding of regulatory requirements for GMP environments based on USP, EP, ISO, PIC/s, EMA & FDA guidance and standards.

There’s no cost to attend, lunch/refreshments will be provided and you’ll receive a certificate of attendance.

Discussion Topics

• Complying with the revised EU GMP Annex 1
• Best practices for compliant air particle counting
• FDA guidelines on data integrity (ALCOA / 21 CFR Part 11)
• Clean-in-place and cleaning validation with TOC analyzers
• European and US Pharmacopeias requirements for TOC and conductivity measurements
• Making Sense of Cleanroom Regulations (21501, 14644, Annex 1, GMP)

Dates and Locations

• Cambridge, MA, Wednesday, April 23, 9:00 a.m. to 5:00 p.m. Local Time
• Edison, NJ, Tuesday, May 6, 9:00 a.m. to 5:00 p.m. Local Time
• Durham, NC, Thursday, May 8, 9:00 a.m. to 5:00 p.m. Local Time
• Brea, CA, Wednesday, May 14, 9:00 a.m. to 5:00 p.m. Local Time 

Agenda and discussion topics subject to change.