NEW: IQVISION E-Signature

​​​​​​​​​

IQVISION E-Signature helps users to mitigate the potential risks of failed regulatory audits, which is particularly useful for regulated businesses that are required to meet the FDA’s 21 CFR Part 11 i.e. during the manufacturing of food or pharmaceuticals.

Users are able to create and manage controlled audit logs of key data that are accurate, time and date stamped and unalterable.

When manual cha​nges and overrides are required, the E-Signature application allows for changes and overrides to be made by authorised personnel, approved within an agreed escalation chain and then documented in audit files to maintain an accurate record.

  • Conforms to FDA’s 21 CFR Part 11 requirements​
  • Provides controls necessary for compliant Method of Procedure (MOP) and Standard Operating Procedure (SOP)
  • Single or dual-signature control
  • All history and alarms are secured for deletion and acknowledgment
  • Only points requiring additional security need to be licensed

If you are interested in learning more about E-Signature, or any other IQVISION v2.3 feature, you can get in touch with a member of our sales team by completing the form below.

​​​​​​​​​​
​​