TechValidate Research on Clinical Flow Cytometry


Beckman Coulter Customer Statistic

100% of organizations agreed with the following statement:

“Using high-quality reagents, produced under current Good Manufacturing Practice (cGMP), ensures better lot-to-lot consistency, low error rates and reduces the need for retesting.”





About This Data

This data was sourced directly from verified users of Clinical Flow Cytometry by TechValidate.

TechValidate verifies the identity and organizational affiliation of all participants that contribute to published research data. When research participants so desire, we also guarantee their anonymity so that they may share information honestly and freely.

Respondent Details


More Research on Clinical Flow Cytometry