Events Reports Virtual Workshop
April 8 - 22, 2020
12:00 PM - 2:00 PM (ET)

This 4-hour training program will be divided into 2 2-hr sessions, taking place on April 8 and April 22, 2020. These are live broadcasts.

Many people know about nonconformances, many know about CAPAs, but not that many know about how a nonconformance LEADS to a CAPA.
They also don’t necessarily know how to derive data analytics from these systems. What is being proposed is having everything become an “event” and then take it from there to escalation, but essentially all pre-CAPA inputs are handled the same way.
Why not have a standard approach to documenting, investigating, detailing, and resolving?
Even the best college educated folks really don’t know what is expected in the medical device, food and beverage, pharma, pharmacy, biologics and cannabis corporate world, especially when it comes to writing up non-conformances and CAPAs.

Learning Objectives

  • This course is not meant to be comprehensive; however, it is a guide for better use odf the data derived from recording nonconformances (OOT, OOS, Audit observations, Complaints, nonconforming product, etc.) 
  • Attendees will gain knowledge as to a more standardized way of recording, investigating, and resolving nonconformances, as well as use the recorded data to more effectively communicate tracking and trending of issues.
  • They will will also be able to use the data to assign costs of the resolution and be able to present new key performance indicators to executive management.

Course Outline

  1. Problem resolution philosophy (Six Step Problem Solving Process)
  2. Practical application of the problem solving process
  3. Advantages of using a single system of problem investigation and resolution
  4. Actual Event Report Form use
  5. Event Data Analytics
  6. Report form and Data Analytics Side-by-Side Comparison
  7. How and Event turns into a CAPA
  8. CAPA Data Analytics
  9. Cost of Poor Quality Data Analytics
  10. Q&A

Who would benefit from this course:

  • Manufacturing technicians
  • Manufacturing engineers
  • Quality Assurance
  • Regulatory Affairs
  • Mid-level management/supervisors
  • Executive management

CEU Information

Amount of CEUs: 

Certificates will be issued that explain hours of training, CEUs to be issued by license authorizing organization.



What are the registration prices:

  • Early bird registration for 1 participant is $450 - Available until March 18, 2020
    Regular Registration for 1 participant is $650 - After March 18, 2020 

Can I ask questions of the speakers?

  • Yes! you will be able to ask questions of each speaker. You will type your questions into a chat dialog box and the moderator will read it out loud to the speakers.

What happens if I miss the event:

  • There are no refunds or cancellations within 7 business days of the starting date of the event.

Cancellation and Refund Policy:

  • All cancellations must be made via email. Should you not be able to attend the conference, you may have someone else from your organization take your place or use your registration fee as credit towards a future MedTech event. If these options are not possible, you can receive a refund of the registration fee less a 20% processing fee up until 7 business days prior to the conference. There are no refunds for cancellations within the 7 day period prior to the conference or for "no-shows" to the conference.