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3 Is the Magic Number

Canon Virginia kicks off this free webinar telling attendees that they will not be sharing something they don’t already know, but will share a few best practices for getting things right the first time—three steps to improve medical tooling and validation times.

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An initial real-time poll reveals that the greatest hurdle to getting a product to launch is equal across time-to-market, quality and cost reduction … until time-to-market took the lead in the end. With that in mind, Canon Virginia Inc. reviewed three steps to improve these factors:

  • 1. Design for manufacturing (DFM)

    • Design for injection mold tooling (DFIM) is really design for moldability.
    • There are 3 ways DFIM can help reduce costs and time-to-market:
  1. To the moldmaker: improve ease of machining; simplify the mold and win over the customer
  2. To the molder: maintain robust process windows, improve repeatability and quality; speed up validation
  3. To the manufacturer: ensure incoming parts meet specs, reduce assembly processes and enhance product quality
  • 2. Instrumentation and scientific injection molding (SIM)

    • Instrumentation is the process of installing a series of sensors within the mold to provide key data points in the injection molding process.
    • SIM is a disciplined approach to building robust molding processes for repeatability and high-quality outcomes.
  • 3. Part validation

    • A second poll reveals that the two greatest benefits of part validation according to attendees are:

Standardized process

Consistent quality

Repeatability

Clear documentation

  • Part validation verifies that the part quality is repeatable for mass production, ensures part quality meets customer specs and enables the product to move to market with a documented paper trail.

Some questions that were discussed during the Q&A include:

  • How do you balance gross mold adjustments using an unvalidated process during initial mold sampling vs fine-tune adjustments after the process is validated? 
  • How far should you go in adjusting the mold before SIM begins?
  • What type of support does Canon provide at the start of production?
  • What if I’m not getting the same results?
  • What guidelines do you use to perform DFM?
  • Is DFM/DFIM always done in-house?
  • Is this a service Canon provides?
  • What are the most common problems that you run into when validating manufacturing processes?
  • How do I know if the process has been validated correctly?
  • What are the benefits of process validation over inspection of the final product?
  • How do I decide which one is best?
  • Do you go through a checklist during part and tooling DFM review?
  • Do you prefer direct or indirect (behind the pin) sensor instrumentation?
  • Sometimes changing the machine causes parts being out of spec, poor surface finish, flash, etc. How does Canon address this issue?
  • How do you determine shrink rate for the new materials?
  • Do you have conformal cooling capability for complex tooling?
  • Do you need prototyping to determine shrink rate for new material?

To view this 45-minute webinar, click here

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