Process Failure Mode and Effects Analysis (PFMEA)

Thursday, July 17, 2025
Time: 12:00 PM PDT | 03:00 PM EDT
Duration: 60 Minutes
IMG Chaitanya Baliga
Id: 90659
Live
Session
$119.00
Single Attendee
$249.00
Group Attendees
Recorded
Session
$159.00
Single Attendee
$359.00
Group Attendees
Combo
Live+Recorded
$249.00
Single Attendee
$549.00
Group Attendees

Overview:

PFMEA is a methodical approach used for identifying risks on process changes. The Process FMEA initially identifies process functions, failure modes their effects on the process. 

Why you should Attend:

Process Failure Mode Effect Analysis is a risk management tool to be used in understanding process risk during product manufacturing or services.

Areas Covered in the Session:

  • Understand the P FMEA
  • Understand how to identify failure modes
  • Understand how to assess and prioritize risk associated with product and process using severity, occurrence and detection rankings
  • Understand the challenges associated with product and process
  • Through the recognition and evaluation of potential areas of failure,  identify preventative actions and minimise the risk of failure

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).