J-Pharma

J-Pharma is a modular ERP, integrated with Revorg’s solutions for the hospital and pharmacy channels, management of sales representatives and conferences, and commercial data analysis. Ready for validation, it has innovative features to meet the actual needs of Life Sciences companies with whom we have been working for over 40 years.

Select Life Sciences experts.
We specialize in organizational consulting of business processes and in the development of customized software for the pharmaceutical, diagnostic, and medical device sectors.
Trust a team of sector professionals.
A team of specialists will be available for you, organized in two different areas of competence, and dedicated to production processes and sales, respectively.
Your 100% Compliant ERP for Pharma. J-Pharma J-Pharma manages manufacturing and distribution processes of pharmaceutical companies. It meets FDA, CFR 21 Part 11, GMP and Annex 11 requirements, with specific features for data tracking, audit trail, batch traceability, and management of approval flows. It meets information system validation requirements.

  • PRODUCTION RECIPE (BOM)

  • Setting expiry dates
  • Setting application coefficients on standard batch quantities or decimal multiples
  • Approval of BOMs and Recipes
  • Titration management and side-effects assessment

  • PICKING

  • Use of compounds depending on titration
  • Stocking for the department and picking from stock
  • Assigning compounds from stock availability or semi-finished products under production or starting materials under test
  • Returns from department

  • WAREHOUSE

  • Authorized accesses for handling and/or storage
  • Authorization to handle rejected, quarantined, or expired batches
  • Optical reader for package handling

  • PRODUCTS

  • Modular definition of product properties
  • Management of products going through the weighing room
  • Assignment of deadlines and monitoring
  • Modular batch numbering configuration
  • Assignment of bill of materials, work cycle, department, and warehouse
  • Products subject to QC approval (quality control), released by QP (qualified person), released for shipment

  • BATCHES

  • Batch management from qualified suppliers
  • Incoming materials: checking and traffic light color labeling
  • Batch status management: quarantined, sampled, approved or rejected, released and ready for shipment
  • Management of production date, shelf-life, best-before date
  • Titration management
  • Internal and supplier’s batch identification
  • Batch traceability

  • PRODUCTION

  • Use of approved recipes
  • Management of weighing orders
  • Recording of data and final times
  • Recording of used, discarded or returned materials
  • Quarantine placement of semi-finished or finished product
  • Preventive and final production order evaluation

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