Enabling compliance for electronic records and signatures
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 criteria for using electronic signatures. The optional 21 CFR Part 11 software module of our MACSQuantify Software enables this by:
Seems like you are coming from USA!
Do you want to visit our website in your country?