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Dosage Form Manufacturing

In today's business environment, competition among commercial pharmaceutical manufacturers is becoming more intense. Companies are faced with price erosion due to changes in healthcare practices and government regulations. Under these conditions, manufacturers must improve process efficiency, and better utilize physical and intellectual assets in order to achieve and sustain financial results.

Honeywell’s automation solutions for drug manufacturers improve manufacturing performance by ensuring products are manufactured the right way, at the right time, every time. They provide the electronic management of batches, resources, materials and equipment to ensure that all instructions take place in accordance with specifications. They control and track all aspects of production, enforce Good Manufacturing Practices (GMP) and provide a complete history for regulatory compliance. Benefits achieved by implementing Honeywell solutions include:

  • Improved throughput
  • Reduced operating costs
  • Reduced  validation costs
  • Faster product release
  • Improved manufacturing flexibility

Honeywell solutions allow you to manage every step of the production process, from materials receipt to product shipment. They ensure your manufacturing operations are capable of delivering on your production commitments. Our solutions organize and automate the process of planning, sourcing, producing and delivering new products from concept to commercial manufacturing. Functionality includes:

  • Enterprise-level specification and recipe management
  • Order and batch management
  • Materials management
  • Weigh and dispense operations
  • Exception and deviation management
  • Asset tracking
  • Equipment status management
  • Quality data management
  • Electronic signature compliance (21 CFR Part 11)
  • Electronic batch records
  • Materials traceability and genealogy

Honeywell solutions help minimize the risks associated with maintaining compliance and the high cost of being late to market. Our integrated automation solutions allow you to meet current and emerging regulatory requirements placed on your process, such as GMP, 21CFR Part 11 and GAMP, as well as internal documentation and traceability guidelines.

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