Clinical Supplies Manufacturing and Drug Development Solutions from Honeywell

This description pertains to the processes of Drug Development and Manufacturing of Pharmaceutical Supplies supporting Clinical Studies.

For Solutions for Commercial Pharmaceutical Manufacturing, Biologics Manufacturing, or Regulated Consumer Packaged Goods Manufacturing, click on the appropriate left-hand sidebar button under Solutions.

Developing and introducing a new pharmaceutical product is expensive and time consuming. A delay of even one day can translate into millions of dollars lost. Pharmaceutical companies are looking for ways to reduce time-to-market to maximize the window that the product can be manufactured and sold while it is still under patent protection. Honeywell's Clinical Supplies Manufacturing Solutions effectively specify, control and manage the production and tracking of all materials associated with clinical supplies. Honeywell's Clinical inventory management and recipe-based, interactive electronic batch record capabilities reduce time-to-market and cost of compliance while increasing the efficiency of traceability and reporting.

Implementation of Honeywell's integrated solutions for Clinical Supplies Manufacturing provide the agility needed to stay ahead of the competition and respond quickly to changing clinical studies requirements. They also help you avoid maintenance shutdowns and equipment breakdowns that reduce plant up-time. Honeywell integrated compliant manufacturing control relates directly to reducing cycle time in the Drug Development process.

With Honeywell, you can take control of processes and the environment in your regulated manufacturing facility. Our solutions integrate best practices in such key areas as receiving, weigh/dispense, process control, environmental control, packaging, validation—every cost center in the plant. These solutions enable you to link process automation systems to higher-level platforms such as Enterprise Resource Planning (ERP), and find new, unforeseen opportunities to boost performance and drive down costs.

Honeywell can also help minimize the risks associated with maintaining compliance—and the high cost of being late to market. Our automation solutions allow you to meet current and emerging regulatory requirements placed on your process, such as OSHA, FDA Current Good Manufacturing Practices (cGMP), 21CFR Part 11, and GAMP, as well as internal documentation and traceability guidelines.

Honeywell integrated solutions offer a common platform from Drug Development through scale-up to Commercial Manufacturing.

Honeywell's next-generation Process Knowledge System™, Experion PKS™, incorporates the latest plant automation technologies, including FOUNDATION™ fieldbus, HMIWeb—Honeywell's patented human-machine interface technology, Digital Video Manager (DVM) and Asset Manager PKS™ Alert Manager to protect your plant assets. The Experion PKS open, scalable process and environmental control platform supports today's flexible manufacturing strategies. Process Knowledge Solutions™ address the entire spectrum of your automation and business requirements.

Honeywell's Facility Management Solutions provide the information needed to make crucial decisions quickly. At the core of these solutions is our Enterprise Buildings Integrator (EBI) facility management system. This fully-integrated control platform pulls together all core building systems and integrates information from many different enterprise subsystems, from industrial manufacturing and process automation, to financial records, environmental controls and data warehouses.

Our industry-best MES solution (POMS CMS for Clinical Supplies Manufacturing) allows you to manage every step of the production process—from materials receipt to product shipment. Plus, it ensures your manufacturing operations are capable of delivering on your enterprise's e-business supply chain commitments. We also provide an electronic specification solution (e-Spec) for managing the collaborative development and deployment of pharmaceutical product specifications. The system organizes and automates the process of planning, sourcing, producing and delivering new healthcare-related products from concept to commercial manufacturing. The POMS eSpec specification tool is the facility which integrates material and process specifications from pre-clinical to commercial manufacturing.

By integrating best practices with quality and regulatory compliance, Honeywell Clinical Supplies Manufacturing Solutions give you the means to minimize risk, increase throughput, streamline production costs, and eliminate unnecessary time delays during new product launch.

The left-hand sidebar on this page lists Honeywell products that are particularly appropriate for use in the Clinical Supplies Manufacturing Industry. Please click on those products of interest for more detailed information.