MACS PICK UP POINT Technology
MACSQuantify™ 21 CFR Part 11 option
The Subpart 11 of the Code of Federal Regulations Title 21 (21 CFR Part 11) defines the requirements for submitting electronic records to the FDA as well as the criteria for using electronic signatures. Our optional 21 CFR Part 11 software module of the MACSQuantify™ Software enables this by:
21 CFR Part 11 compliant MACSQuantify V2.10 additional PC license
21 CFR Part 11 compliant setup of MACSQuantify V2.10
MACSQuantify Software, additional license
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