Tag: 21 cfr part 11

21 CFR Part 11 is the FDA guideline that defines the criteria under which electronic records and electronic signatures are considered to be trustworthy, reliable and equivalent to that of... Read More

Freyr SPL/SPM Software is an cost-effective solution for your SPL/SPM submissions which has Automated Process for new SPL/SPM submissions and revisions, adheres with 21 CFR Part 11 HL7 standards. Freyr SPL/SPM... Read More