Pharmaceutical

• Material Receipts against Orders
• Approval & Rejection of Materials by Quality Control
• Label Printings from the system
• A R No. assigning against various batches.
• Stock Status such as Quarantine, Rejection, Approved
• Stock issues based on system generated requisition as per standard formulas.
• Validations on issue of expired based material & as per FEFO (First Expired First Out)
• A.R.No. Status
• Retesting of Materials as per Retest Over Due Report
• Conversion of various grades on approval of Quality Control
• Excess Return from Production, Material Transfers & Stock Adjustment
• Additional Requisition of materials for Producton.
• Issues for Job Work & Return (Third Party Job Work)
• Stock Goods in Process
• Production Delivery to various stages & BSR
• Cost Estimation
• ATR (Analytical Test Report) & FPRR (Finished Product Release Report) from the system
• Bill of Material for Raw Material & Packing Material
• Quarantine, Approval
  

You are aware that for any Pharmaceutical ERP, compliance with GMP & FDA requirement considered as prime importance. Though 21 CFR Part II has been launched, many companies yet to tackle its practical implementation. User-friendly GSeven’s ERP Solution is compliant to all statutory regulation & as per the guidelines of 21CFR Part II and it is quick to implement.