Take Control of Pharmaceutical Manufacturing with an Industry-Specific ERP

Digitally record every batch, from formulation and material consumption to yield and quality checks, eliminating errors and ensuring audit-ready traceability.

Enforce compliance with US FDA and global regulations through electronic signatures, secure access controls, and detailed audit trails across the manufacturing process, from material issue to batch release.

Schedule in process, stability, and shelf-life testing for raw materials and finished products. Define test parameters, record and analyze results, manage retesting schedules, and automate pass/fail workflows to ensure consistent quality.

Automatically generate COAs at batch completion or during dispatch, integrating QC test results to meet customer and regulatory requirements with seamless documentation.

Manage and track inventory with FEFO logic, shelf-life monitoring, and expiration alerts. Get real-time visibility with barcode scanners, RF devices, mobile WMS, and electronic scales.

Streamline product development from R&D trails and batches to commercialization with version-controlled formulations, test results, and cost vs yield performance comparisons.

Track real-time batch-wise costs, including raw materials, utilities, labor, and overheads. Calculate actual vs standard cost variances to identify production inefficiencies and increase margins.

Manage campaign, super batch, and sub-batches across facilities. Digitally capture SOPs and shop-floor activities with integrated weigh sheets and MES tools.

Effectively manage customer-supplied APIs, client-specific formulations, and private labeling with secure portals for order and COA tracking. For own-brand operations, integrate with D2C platforms like Shopify and others.

Automatically generate serial numbers for items and pallets based on customer-specific requirements. Ensure every unit is uniquely identified, traceable, and compliant with global serialization mandates.

Capture and trace critical quality and process data in real time, including medication details, lab timings, temperature readings, and other key process indicators.

Create and manage regulatory documents such as Globally Harmonized System (GHS) labels and Safety Data Sheets (SDS) to meet international compliance standards. BatchMaster ERP provides smooth integration with LISAM to manage these document compliances.