4-Hour Virtual Seminar on Risk Management Training with DFMEA and PFMEA

Id: 90662
Recorded
Session
$395.00
Single Attendee
$745.00
Group Attendees

Overview:

Failures are prioritized according to how serious their consequences are, how frequently they occur, and how easily they can be detected. The purpose of FMEA is to take actions to eliminate, reduce, and/or mitigate failures, starting with those deemed highest priority. FMEA can be used during design (DFMEA) to prevent failures. Later, it can be used for process control (PFMEA), as well as before and during ongoing operations. Ideally, FMEA begins during the earliest conceptual stages of design and continues throughout the life of the product or service. FMEA has bigger leverage and impact in the early stages of development when changes are less costly to implement.

Why you should Attend:

FMEA is a type of risk assessment that uses a step-by-step approach to identify potential failures in a design, process or a product or service. This identification allows for analysis to prevent or reduce future failures. “Failure modes” refers to the ways in which something can fail. DFMEA helps prevent design-related issues from reaching production, while PFMEA helps prevent process-related issues from affecting the final product. Both are crucial for delivering a high-quality product and minimizing risks. 

Areas Covered in the Session:

  • Risk Management 
  • Failure Mode and Effect Analysis
  • Design Failure Mode & Effect Analysis (DFMEA) :Boundary Diagram, the P-Diagram (Parameter Diagram), the
  • DFMEA Worksheet, and the Design Verification Plan & Report (DVP&R)
  • Process Failure Mode & Effect Analysis (PFMEA) : The P-Diagram, or Parameter Diagram The Process Flow
  • Diagram (PFD) the DFMEA Worksheet and Control Plan 
  • Implementation - Do's and Don'ts 
  • A look into the future of Risk Management and FMEA

Who Will Benefit:

  • Quality Engineers/Specialist/Managers, Manufacturing/Operational supervisors and managers, and Procurement Managers
  • Regulated industries like pharmaceuticals, medical devices, nuclear, biotech, natural health products, food, equipment, and nuclear.

Speaker Profile

Dr. Chaitanya Baliga has over 20 years of experience in quality management systems, regulatory compliance, and supplier management in industries, such as consumer products, medical device, pharmaceuticals, automotive, and toys. One of Chaitanya’s responsibilities is ensuring quality and compliance activities pertaining to manufacturing of regulated products (drugs, natural health products, cosmetics, and medical devices).