Pharmaceutical & Healthcare Products
⚠️Common Process Problems
Batch manufacturing record (BMR) manual filling
Regulatory reporting takes days to compile
Deviation and CAPA tracking on spreadsheets
Temperature and environmental monitoring gaps
Annual Product Review (APR) data collection nightmare
Supplier audit and qualification documentation
Stability study data management chaos
AI-Powered Automation Solution
Digital BMR & Documentation
Electronic batch manufacturing records, real-time data entry validation, automated signature workflows, and complete audit trail
Regulatory Compliance Suite
Automated regulatory reporting (Schedule M, Form 27, etc.), deviation and CAPA tracking with workflows, and APR data auto-compilation
Environmental Monitoring System
Automated temperature/humidity logging, real-time alerts on deviations, and integration with cold chain tracking
Supplier & Quality Management
Supplier audit tracking, COA (Certificate of Analysis) management, and stability study data repository
📊Expected Business Impact
BMR preparation time reduction
regulatory reporting time (vs 2-3 weeks)
audit-ready documentation
missed environmental deviations
Investment & Timeline
Typical Investment
₹6-10 lakhs
Implementation Timeline
10-14 weeks
Expected ROI
6-9 months