Engineering Document Intelligence
for Hyderabad & Telangana
Domain-native engineering document AI for Hyderabad's pharmaceutical, specialty chemical, defence engineering, and PSU engineering cluster. P&ID extraction, piping MTO, instrument index automation, with GMP, 21 CFR Part 11, IBR, and PESO compliance native to the workflow.
Serve Hyderabad pharmaceutical majors (Dr Reddy's, Aurobindo, Divi's, Granules, Natco, MSN) with GMP-grade P&ID digitisation and compliance automation
Specialty chemical plants across Hyderabad / Medak / Jeedimetla / Bollaram / Patancheru industrial corridors
BHEL Ramachandrapuram (boilers manufacturing): IBR Form III register automation and weld schedule generation for pressure vessel supply
NFC (Nuclear Fuel Complex) Hyderabad: engineering document digitisation with restricted-access workflow
BDL (Bharat Dynamics Limited) and ordnance / defence engineering: classified document handling with compliance registers
21 CFR Part 11 compliant document extraction for Hyderabad pharma exporters to US / EU markets
OSD / injectable / API plant commissioning: engineering deliverables in pharma-native format for regulatory submissions
Telangana PESO compliance for compressed gas and solvent storage across Hyderabad industrial estates
Why is Hyderabad important for Pathnovo?
Hyderabad is India's pharmaceutical capital (accounting for ~40% of national pharma production) plus a major specialty chemicals, defence engineering, nuclear fuel, and PSU engineering hub. Every pharma facility operates under GMP, USFDA, WHO, and 21 CFR Part 11 requirements; engineering documentation is a regulatory deliverable, not just an engineering artifact. Specialty chemical plants concurrently require PESO hazardous-area compliance, IBR pressure-equipment registers, and state Factories Inspectorate filings. BHEL Ramachandrapuram supplies IBR-certified boilers globally. Hyderabad needs full-stack engineering document intelligence with pharma and industrial compliance depth.
Does Pathnovo support GMP and 21 CFR Part 11 compliance?
Yes. Pharma clients (Dr Reddy's, Aurobindo, Divi's, Granules, Natco, Hetero, Laurus, MSN) operate under GMP, USFDA, WHO, and 21 CFR Part 11 for electronic records. Pathnovo's engineering document extraction preserves evidence chains, maintains audit trails for each extracted field, and formats outputs for regulatory submission. The platform complements GMP QMS tools (Veeva, Documentum, MasterControl) with engineering-domain extraction intelligence the QMS systems cannot provide.
Which Hyderabad operators does Pathnovo work with?
Pharmaceutical: Dr Reddy's Laboratories, Aurobindo Pharma, Divi's Laboratories, Granules India, Natco, Hetero Drugs, Laurus Labs, MSN Laboratories, Neuland, Mylan, Hospira. Chemicals: specialty chemical plants across Jeedimetla / Bollaram / Patancheru / Nalgonda. Heavy industry: BHEL Ramachandrapuram (IBR boiler supply), NFC (Nuclear Fuel Complex), BDL (Bharat Dynamics Limited), ECIL. PSU engineering: Engineering consultancies serving PSU projects nationwide. EPC contractors headquartered in Hyderabad serving Andhra / Telangana / national projects.
How does Pathnovo handle pharmaceutical engineering documents specifically?
Pharmaceutical plants present unique engineering documentation challenges: cleanroom classifications (ISO 14644), HVAC design records, utility validation (water for injection, compressed air), process equipment qualification (IQ/OQ/PQ), cleanability studies, cross-contamination risk assessments. Pathnovo extracts across all these document types alongside standard EPC deliverables (P&IDs, isometrics, datasheets, HAZOP). The output supports both engineering handover and regulatory submission workflows.
What is pricing for Hyderabad clients?
Pathnovo uses credit-based pricing invoiced in INR with GST by Pathnovo India Pvt Ltd, full platform included on every paid tier (Starter, Professional, Scale, Enterprise). Pharma-sector specific rate-card compatibility available on top of the tier subscription. Free 14-day trial with 100 credits, no credit card. Major pharma operators with 10-50+ facilities typically move to Enterprise on 3-year contracts, scoped on consolidated asset count and regulatory scope (GMP + FDA + 21 CFR Part 11 + IBR + PESO combined compliance). See our pricing page for full plan details.
See what your documents actually contain.
Send us 10 documents from your current project. We extract, reconcile, and show you exactly what we find in 48 hours, before any contract.
If the accuracy isn't what we promised, you owe us nothing.