Prismatic Pharma ERP ensures strict GMP compliance, automated batch manufacturing records (BMR), expiry management, quality assurance, and DRAP regulatory tracking.
Pharmaceutical manufacturers face severe compliance risks, batch quarantine errors, formula confidentiality leakage, and recall difficulties without validated ERP software.
Prismatic ERP enforces strict digital quality gates — from raw API sampling and quarantine release to master formula versioning and FEFO warehouse dispatch.
Purpose-built modules configured for your industry — not a generic system retrofitted to fit.
Automated electronic BMR/BPR documentation with yield calculations & electronic signatures.
Active Pharmaceutical Ingredient (API) quarantine, QC sampling, and potency-based dosing.
Strict First-Expiry-First-Out picking enforcement for finished formulations.
Certificate of Analysis (CoA) generation, stability testing logs, and quarantine holds.
Encrypted master recipe vault with strict version controls and change log audits.
Built-in audit trails, DRAP price control logs, and GMP batch release checklists.
Manage pharma distributors, break-bulk discounts, bonus schemes, & credit limits.
Instant 1-click batch trace to identify all customer invoices in case of a product recall.
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