The Toximaster® FQC1 Software supports data processing based on the protocols complying with three types of pharmacopeia (USP, EP, JP) for bacterial endotoxin testing. This software is compliant with FDA 21 CFR Part 11 ERES (electronic records/electronic signature), which requires the proper information from all parties involved in the testing of the sample. Toximaster® FQC1 offers excellent audit trail capabilities, can provide statistical processing of means, standard deviations, and has robust data processing functions. The data processing functions can be performed by defining sample types such as standards, controls and test samples.
Catalog No. |
Model |
Contents |
290-36831 |
Toximaster®️ FQC1 PC Set E |
Toximaster®️ FQC1 Software PC Set |
298-36871 | Toximaster®️ FQC1 Software | Toximaster®️ FQC1 Software Alone |
Q: What type of audit trail capabilities are available with this system?
A: The Toximaster® FQC1 Software is capable of various types of audit trails:
Q: Can the protocols and standard curves be saved for later use?
A: Yes, the Toximaster® FQC1 Software can save and archiving information for later use.
Q: Will each user have their own unique identification (username and password) to access the software?
A: Yes, the Toximaster® FQC1 Software can save each user with unique identifier and password access, specific to their role in your lab. The system administrator can customize user privileges in the system.