Audit-ready compliance for pharma, finance and tax
Every test, release and deviation is recorded and ready for inspection. ParaTech Pharma ERP bakes regulatory and tax controls into the same transaction flow your plant already runs.
Regulatory confidence, out of the box
DRAP Readiness
Batch records, CoA and traceability structured for DRAP inspections.
WHO-GMP Readiness
Quality gates, deviation control and electronic signatures across the plant.
USFDA-Oriented Controls
21 CFR Part 11-ready electronic signatures and locked audit trails.
FBR Digital Invoicing
Real-time invoice transmission and POS compliance with QR receipts.
IFRS / IAS Reporting
IAS-1, IAS-2, IAS-7 and IFRS-15 native reporting and inventory costing.
User-Level Controls
Role-based access, approval workflows and full audit trails everywhere.
Inspection-ready, every day
No scramble before an audit. The evidence regulators ask for is already captured, signed and locked.
- QA/QC audit trail
- Electronic BMR / BPR
- Batch & lot traceability
- Certificate of Analysis
- Stability studies
- FBR Digital Invoicing
- FBR POS where applicable
- IFRS / IAS reporting
- IAS-2 inventory costing
- User-level access controls
- Approval workflows
- Locked audit trails
| Test | Specification | Result | Status |
|---|---|---|---|
| Description | White uncoated tab. | Conforms | OK |
| Assay (%) | 95.0 – 105.0 | 99.4% | OK |
| Dissolution | 80% @ 30 min | 94% | OK |
| Hardness (kp) | 4.0 – 8.0 | 6.2 | OK |
| Disintegration | 15 min | 9.4 min | OK |
Released by QA Manager · Signed Electronically · Audit Trail Locked · Multi-format export (PDF / Word / Excel)
Prepare for your next audit with confidence
See ParaTech Pharma ERP in action on your real-world scenarios — batch traceability, QA release, FBR invoicing and batch profitability.