ComplianceOnline

4-hr Virtual Seminar: Design Reviews for Efficiency and Efficacy

Instructor: Dev Raheja
Product ID: 702028
  • Duration: 4 hrs

Training CD / USB Drive

$799.00
One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-565-8542

Email: customercare@complianceonline.com

Read Frequently Asked Questions

This 4 hour training will focus on best practices in design reviews and show how you can add high value to your products and processes by improving the performance while reducing the life cycle costs significantly.

Why Should You Attend:

Is your organization making too many engineering changes? Would you like to prevent this waste of engineering resources and time?

The techniques discussed in this webinar will make you aware of the primary source of mistakes--the user requirements specifications.

Evidence shows that as much as 60 percent requirements are overlooked in the specifications. Such oversights result in inefficient and ineffective products and processes. The speaker, with experience on hundreds of new products, will show you how to discover the unspecified needs of the customers through creative design review methods. A company prevented over 700 engineering changes using these techniques resulting in reduced budgets and finishing the project ahead of time.

This webinar will show how you can add high value to your products and processes by improving the performance while reducing the life cycle costs significantly

Agenda: (All time in EDT):

  • 12:00 - 12:15 Principles of design reviews
  • 12:15 - 12:25 Efficiency gaps in design control
  • 12:25 - 12:45 Efficiency gaps in manufacturing controls
  • 12:45 - 1:00 Methods of improving efficacy in product design
  • 1:00 - 1:15 Methods of improving efficacy in process design
  • 1:15 - 1:30 Organizing and managing design review teams
  • 1:30 - 1:40 Best practices in design reviews
  • 1:40 - 1:55 Cost reduction techniques
  • 1:55 - 2:10 Break
  • 2:10 - 2:30 Design reviews for software in the product and processes
  • 2:30 - 2:45 Design validation planning for efficiency
  • 2:45 - 3:00 Process validation planning for efficiency
  • 3:00 - 3:15 Retrospective validation planning for design and process efficacy
  • 3:15 - 3:30 Identifying management gaps to improve design efficiency
  • 3:30 - 3:40 Tracking design control requirements through design reviews
  • 3:40 - 3:50 Tracking life cycle cost reduction to assure meaningful use of reviews
  • 3:50 - 4:10 Attendee discussions and questions

Areas Covered in the Seminar:

  • Efficiency issues in design control.
  • Efficiency issues in manufacturing processes.
  • Efficacy issues in product design.
  • Efficacy issues in process design.
  • Design review fundamentals.
  • Team management requirements.
  • Best practices in design reviews.
  • Software design reviews.
  • Cost reduction techniques.
  • Design validation planning for efficiency.
  • Process validation planning for efficiency.
  • Retrospective validation planning for efficacy.
  • Identifying management gaps to improve efficiency.
  • Tracking design control requirements through design reviews.
  • Tracking life cycle cost reduction.

Who Will Benefit:

Manufacturing and engineering professionals across all industries will benefit from this webinar.

  • Quality Assurance
  • Design Engineers
  • Manufacturing and Production Engineers
  • Product Managers
  • Managers in Manufacturing and Production
  • Marketing
  • Safety Engineers and Managers
  • Regulatory Affairs

Instructor Profile:

Dev Raheja, is a respected and sought out expert on medical device and patient safety. He draws on his 25 years of experience as a risk management and product assurance consultant to provide medical device stakeholders with a systematic way to learn the science of safety and reliability. He uses evidence-based safety theories and tools taken from the aerospace, nuclear, medical, and chemical industries to identify the combination of root causes that result in an adverse event.

He applies analytical tools that can effectively measure efficiency and efficacy. His focus is on using various types of innovations to encourage a culture conducive to high return on investment.

He is the author of the books Assurance Technologies principles and Practices, and Safer Hospital Care. He has served as Associate Professor for the PhD degree program in Reliability Engineering at University of Maryland during 1994-99. He has received several awards including the Scientific Achievement Award from the International System Safety Society.

Follow us :
Upcoming In-person Seminars by EX-FDA OFFICIALS
FDA's Medical Device Software Regulation Strategy

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email customercare@complianceonline.com call +1-888-717-2436 (Toll Free).

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