Seabrook Technology Group today announces its schedule for a series of webinars to be held in 2017.
Seabrook Technology Group today announces its schedule for its webinar series to be held in 2017, beginning on January 10th on how Paperless Manufacturing can set the standard with quality and compliance for medical device manufacturers.
Discussion within this Webinar will include:
- FDA Non-Compliance Quality Subsystem Observations.
- Outcomes for failing to comply.
- 10 x Rule for Defects in a Manufacturing Process.
- How CAMSTAR MES fits into the FDA Case for Quality Model.
- Why 8/10 top medical device manufacturers use CAMSTAR.
- An FDA presented case for Paperless Manufacturing – electronic systems supporting quality.
Future webinars will be provided on the following topics:
Click Here to register now for our complementary webinar