CapabilityAI & Intelligent Automation
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AboutThe team behind the work
Keep Regulatory Records and Operations in Step.
Registration dossiers, manufacturing records, SOPs and product and site documents often live in different systems. Tech Tammina Pharma Compliance brings them together, compares them and manages every gap through a controlled, auditable workflow.
What Is Pharma Compliance Automation?
Pharma compliance automation uses document intelligence and workflow to check that manufacturing, product and site information matches what is registered with regulators. Tech Tammina’s solution compares regulatory and operational documents, flags mismatches, routes them through review and change control, and keeps a complete audit trail for inspections.
Why Regulatory and Manufacturing Records Drift Apart
A change on the manufacturing floor must match the registered details for every market. But the information is spread across documents, teams and systems. Manual comparison is slow and hard to prove during an inspection.
Every market
A floor change must match registered details for every market.
Scattered records
Information sits across documents, teams and systems.
Slow comparison
Manual comparison takes too long.
Hard to prove
Evidence is difficult to show during an inspection.
How Pharma Compliance Automation Works
Collect
Bring in registration, manufacturing, SOP and product and site documents.
Extract
Capture key attributes such as materials, processes, specifications and sites.
Compare
Detect differences between registered and operational information.
Assess
Classify each gap by product, market and impact.
Route
Send findings to regulatory, quality and site teams.
Resolve
Track actions through change control or deviation workflows.
Report
Dashboards and inspection-ready records of every decision.
Key Capabilities for Regulatory and Quality Teams
Document Comparison
Side-by-side comparison with highlighted differences.
Product and Site Compliance
Compliance status by product, site and market.
Deviation and Change Workflows
Structured handling of findings, approvals and actions.
Audit Trail
Time-stamped history of data, reviews and approvals.
Designed for GxP-Regulated Environments
The workflow supports controls commonly expected in GxP settings, including role-based access, audit trails, controlled approvals and validation documentation. AI assists with reading and comparing. Qualified people make every regulatory decision.
What You Can Measure
Measure
Time to compare and assess documents
Measure
Open compliance gaps and their age
Measure
Inspection preparation effort
Measure
Consistency of records across markets
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SolutionPharma Compliance FAQs
Straight answers to the questions buyers ask most.
What Is Pharma Compliance Automation?
Pharma compliance automation uses document intelligence and workflow to check that manufacturing, product and site information matches what is registered with regulators. Tech Tammina’s solution compares regulatory and operational documents, flags mismatches, routes them through review and change control, and keeps a complete audit trail for inspections.
How do we know our manufacturing data matches what we registered?
The solution compares registered and operational documents and highlights every difference for review.
Does the AI make regulatory decisions?
No. It reads and compares. Qualified regulatory and quality staff make every decision.
Is the solution Part 11 compliant?
Compliance depends on your validated implementation. The workflow supports audit trails, access control and controlled approvals, and we support your validation activities.
Will it help us prepare for inspections?
Yes. It keeps a time-stamped record of findings, reviews and actions, ready for inspectors.
See Pharma Compliance working on your documents.
Book a working session with our team. Bring real samples — we will show you the flow, the controls and the outcomes you can measure.