GMP-compliant pharmaceutical manufacturing with batch records, stability testing, DFTQC/DDA compliance, clean room management, and full Nepal regulatory support.
Complete GMP-compliant solution for Nepal pharmaceutical companies
Electronic BMR with step-by-step process instructions, in-process checks, yield tracking, and deviation management.
WHO-GMP documentation, DFTQC submission forms, DDA license tracking, and regulatory audit trail.
Stability study schedules, accelerated and long-term testing, in-process QC, and Certificate of Analysis generation.
Environmental monitoring, differential pressure logs, personnel gowning records, and area clearance management.
Approved vendor list, quarantine management, sampling procedures, potency tracking, and expiry-based FIFO.
Batch-wise costing, overhead allocation, VAT/excise duty, TDS management, and IRD-compliant reporting.
Full regulatory documentation
Electronic records speed reviews
Raw material to finished product
Stay inspection-ready always
Join 100+ pharmaceutical companies across Nepal using M AND R SOLUTION. Start your free 30-day trial today.