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Compliance Training Panel.

Compliance Training Panel provides Quality trainings through their world class platform which enables the clients to discuss with industry experts and to gain related information.

Compliance Training Panel has been established by professionals in the field of Quality, Compliance Auditing and Health Care, Education & Finance with an objective to create an ecosystem that will deliver quality training's on compliance of various regulatory and legal requirements.

We are a US based organization specializing in online trainings in the form of Webinars and Seminars.

Eliminating Production Defects: Cheaper and Faster
Description :
The average number of medical device recalls is more than 3 per day!

A very high percentage of recalls is because of manufacturing defects such operator error, too much variability in the production process, wrong labeling, wrong parts in kits, and wrong stress testing in production. Companies spend millions of dollars on warranties not knowing that almost all warranty failures from flawed manufacturing. Most of these defects can be prevented by changing the product and component design by design engineers, and by procuring reliable and maintainable production machinery.

Objective :
Most of the blame lies with management according to Dr. Edward Deming, the famous quality guru who guided Japan to become Number One in quality. Management needs to set Zero Defect as the only standard of performance. Management must provide policies and procedures for doing right things, right way, at right time. That includes design engineers who must design out causes of manufacturing defects. This can be done for eliminating over 90% manufacturing defects and stop manufacturing departments from buying wrong production machines.

Areas Covered in the Session :
  • Zero defects should be the only standard of performance in manufacturing
  • Types of flaws in manufacturing requirements
  • Doing right the first time results from management leadership
  • Heuristics for designing out manufacturing defects
  • Manufacturability analysis during device design
  • Establishing key critical product characteristics for production managers
  • Process analysis tools
  • Process Failure Mode and Effects Analysis
  • Avoiding Failure Mode and Effects Analysis mistakes
  • Defect mitigation methods
  • Fault Tree Analysis, a world class practice for defect prevention
  • Examples of world class defect elimination practices
Who Will Benefit:
  • Senior management
  • Manufacturing managers and engineers
  • Production managers and engineers
  • Entire engineering staff
  • Test engineering staff
  • Regulatory affairs professionals
  • Marketing Managers
  • Service managers
  • Project Managers and engineers
  • Quality Assurance staff
  • Product safety staff
About Speaker:
Dev Raheja, MS,CSP, is an international Risk Management and Quality Assurance consultant specializing in the field of Healthcare, medical device, and aerospace industry. He has held various positions in GE Healthcare, Cooper Industries and Booz-Allen & Hamilton. He is a trainer, author of the books Safer Hospital Care, Assurance Technologies Principles and Practices, and Design for Reliability. In his 25 years consulting experience he has conducted various training programs across various geographies. Currently he is an Adjunct Professor at the Florida Tech for its degree in Healthcare Management, and serves on the Patients and Families Advisory Council at Johns Hopkins Hospital. He is Associate Editor for Healthcare Safety for the Journal of System Safety, and is a member of the American College of Healthcare Executives.
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