Significant benefits that Pharmaceutical companies can achieve by implementing Sage X3 ERP software are:
- Real-time bi-directional material traceability
- Quality management
- Compliance & Traceability management
- Wastage elimination through expiry alerts
- Lab testing management
- Management information reporting
- Batch tracking
- Formulation & packaging
- Better customer relationships
- Costs & analysis
- Process and mixed-mode manufacturing
- Formula management
- Weighing scales (optional)
- Product packaging
- Work schedule management
- MPS/MRP
- Technical data configuration
- Costing
- Quality assurance
- Capacity planning
- Multi-level warehousing: location, lot, and sub lot control
- Forward and backward lot traceability
- Product serialization
- Shelf life management with expiration date control
- Movements and transactions
- RF data acquisition
- Quality control
- Costing
- Physical counting
- Replenishment
- Purchase requisitions
- Encumbrance accounting
- Requests for proposals
- Purchase orders
- Multi-level approval processing
- Sub-contracting
- Invoice tracking
- Sophisticated pricing and contract management
Supplier returns
- General ledger
- Budgeting
- Allocations
- Fixed assets
- Analytical accounting
- Project accounting
- Accounts receivable / Accounts payable
- Open pricing
- Quotes and contracts
- Order entry
- Product configuration
- Inventory allocations
- Delivery scheduling and shipping
- Invoicing
- Customer returns
- Sales commissions
- Marketing campaigns
- Sales force automation
- Customer support
How Sage X3 will help you solve Pharmaceutical challenges?
Track the real-time location of finished products, their manufacturing date, and expiry date. Set project completion dates. Create product formulas to monitor the batch production process.
Develop and revise formulas using the formula tracking system. Track the lot number of each raw ingredient and of the final manufactured products. Manufacture enormous quantities of drugs in a single run.
Meet the guidelines set by government agencies, regulatory bodies, and international Pharmaceutical watchdogs. Adhere to validation protocols and quality management practices.
Manufacture products of consistent quality. Conduct quality assurance tests, track test results and take corrective actions whenever needed. Also, identify samples for quality control tests using the checkpoint tracking facility.
Track vendors and their pricing variations. Monitor product lead times. Trace the lot number of each ingredient you receive from the vendor and eliminate costs associated with product recalls.