Request a Quote

Automating GMP Cleanroom Routine Monitoring to reduce human error

The videos below show how the fully automated MET ONE 3400+ air particle counter automates cleanroom routine environmental monitoring to reduce human error and improve 21 CFR Part 11 data integrity. Learn more about the Beckman Coulter Life Sciences MET ONE 3400+ portable GMP cleanroom air particle counter. MET ONE 3400+ portable GMP cleanroom air particle counter.

Request a Quote

"How To" Demo Videos

Introduction & accessories

Sample run with pre-configured SOP

Sample run without pre-configured SOP

Adding comments to the ticker tape

Network settings

Start sample run with remote device

Report audit trail

Report samples

LDAP Settings

Calibration certificate

Add & set up user

Add instrument to machine group

Set up SOP

Set up building & map

Set up location

Release SOP

Features of the MET ONE 3400+

21 CFR Part 11 Compliance

This video explains how the MET ONE 3400+ addresses GMP Cleanroom Routine Environmental Monitoring 21CFR part 11 data integrity challenges.

Stay up to date with our newsletter

Receive timely updates on your favorite topics from the experts at Beckman Coulter Life Sciences

© 2000-2024 Beckman Coulter, Inc. All rights reserved. Beckman Coulter, the stylized logo, and the Beckman Coulter product and service marks mentioned herein are trademarks or registered trademarks of Beckman Coulter, Inc. in the United States and other countries. All other trademarks are the property of their respective owners.

Beckman Coulter Life Sciences

NOT ALL PRODUCTS ARE AVAILABLE IN ALL COUNTRIES. PRODUCT AVAILABILITY AND REGULATORY STATUS DEPENDS ON COUNTRY REGISTRATION PER APPLICABLE REGULATIONS The listed regulatory status for products correspond to one of the below: IVD: In Vitro Diagnostic Products. These products are labeled "For In Vitro Diagnostic Use." ASR: Analyte Specific Reagents. These reagents are labeled "Analyte Specific Reagent. Analytical and performance characteristics are not established." CE-IVD, CE: Products intended for in vitro diagnostic use and conforming to the In Vitro Diagnostic Regulation (IVDR) (EU) 2017/746. (Note: Devices may be CE marked to other directives.) RUO: Research Use Only. These products are labeled "For Research Use Only. Not for use in diagnostic procedures." LUO: Laboratory Use Only. These products are labeled "For Laboratory Use Only." No Regulatory Status: Non-Medical Device or non-regulated articles. Not for use in diagnostic or therapeutic procedures.