Compliance-grade visibility.
Audited operator actions, role-based access, and environmental monitoring for pharmaceutical manufacturing.
- Data integrity expectations across every recorded value
- Audited operator actions demanded by quality systems
- Access control across shifts and roles
- Equipment and environmental monitoring
- Validation documentation requirements
How SCAIQ™ addresses it.
Users/Roles/2FA + Audit
The page's spine — every action attributed and recorded
Historian
Integrity-focused records
Alarms
Environmental excursions, escalation
Reports
Batch/environmental summaries
SCAIQ™ supports customers' compliance programs with a strong audit and access-control foundation — validation and regulatory sign-off remain the customer's responsibility.
Ath Software's delivery of digital batch manufacturing record (BMR) and certificate of analysis (COA) systems for a pharma-adjacent manufacturer reflects domain fluency in this space.
Frequently asked questions
What does the audit trail contain?
User, workstation, timestamp, and (where required) operator comment for every recorded action — logins, security events, page access, and operator actions.
What is the user authority model?
Four cumulative roles with two-factor authentication and configurable password/session policy.
Can SCAIQ™ monitor environmental parameters?
Yes — any tag (temperature, humidity, pressure, etc.) can be monitored, trended, and alarmed like any other process value.
See SCAIQ™ for pharmaceuticals.
Bring your toughest SCADA questions. Our engineers will show you real screens, real alarms, and real trends.
Or talk to us directly: +91 84014 22388 ·sales@scaiq.com