Ensure your project is cost-effective and you receive on-time delivery of every component or product we manufacture.
Medical Manufacturing Project Management
Through a rigorous project management process, Paragon Medical ensures the cost-efficient, on-time delivery of every precision component and product manufactured. Our project management team consists of skilled production and engineering personnel who are dedicated to meeting specific delivery needs. This level of dedication means that machining start times are adhered to and that integrated systems and lean-manufacturing-based project management tools are utilized to track the progress of each order.
From planning and design to tooling and manufacturing commercialization, our engineers have a deep understanding of multiple manufacturing disciplines and process design capabilities to support any project. We can support and manage the entire supply chain process so you can significantly reduce the suppliers involved in the project and simplify validation requirements—even for the most complex products.
In addition, we ensure that delivery timelines remain achievable by quickly determining production challenges and then making the necessary adjustments. We also maintain an open, ongoing dialog with our customers, communicating the status of their projects clearly and frequently.
Competitive Advantages
Not only will you realize improved quality, you’ll also streamline communication, eliminate redundant efforts and establish transparent accountability. Medical device and pharmaceutical manufacturers can leverage our FDA registered facilities to support device submission that will lead to the FDA device listing process. All of these benefits are available under one roof so you’ll get your product to market faster with greater cost efficiency. Other advantages include:
- Multi-discipline engineering expertise to support every aspect of product development, validation and commercialization.
- Dramatic speed-to-market savings.
- Customers can consolidate the suppliers and number of locations to validate.
- Streamlined communications, effort and accountability.
- Easier regulatory reporting: assemblies leave our manufacturing facilities complete and ready-to-use. The device listings can be reported as needed directly to the FDA to support submission
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