ISO 13485:2003 • FDA Registered

Pilot and Full Scale Production

Nexcore will collaborate with your team to get your product manufactured reliably, cost effectively and on time. With solid experience in all phases of medical device development and commercialization, Nexcore is comfortable entering the process at any stage. We have been brought into projects at their inception, midpoint of development. We know just what to look for and sometimes are called upon to rescue manufacturing.

Whether pilot production for clinical trials or full volume manufacturing, Nexcore employs the same stringent manufacturing systems and standards required for medical devices.  All programs coming into Nexcore go through an extensive DFM and Design Transfer process to review every portion of your documentation package. As details are entered into our manufacturing control system, we look for economies of scale, manufacturing efficiencies and forecast end-of-life scenarios for components.

Nexcore will also package and distribute your product, either to your inventory or directly to your customers – another added value for Nexcore clients.

In-house capabilities include:

  • Product design and development
  • Design Transfer
  • Design for manufacturing (DFM)
  • Verification and Validation
  • Manufacturing
  • Fulfillment

Nexcore Technology, LLC
150 Hopper Avenue • Waldwick NJ, 07463 • 201-968-9400 •
©2018 Nexcore Technology, LLC