Course: Adulterated Product Monitoring (APM)

Section outline

Select section Welcome to the Adulterated Product Monitoring (APM) Training course

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Welcome to the Adulterated Product Monitoring (APM) Training course

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Purpose:

This course provides introductory training on the Adulterated Product Monitoring (APM) module of the Public Health Information System (PHIS) that is used to document industry notification that an establishment has shipped or received adulterated product that is in commerce. This course is for FSIS field personnel who are PHIS users, and who may be asked to perform the in-plant portions of the APM function.

Participant instructions:

This training course is available anytime. You are expected to complete the course within approximately 2 hours. Please ensure that you complete the training at your own pace.

The training instructions page that was emailed with your course registration provides additional information on how to navigate and use this course.

Please open the “How to Use Moodle Interactive Content” lesson below to start the course and learn how to navigate the training system features.

There are no grades for this course. Click on the topics below one-by-one to view the material. You will also find regulation and directive references at the bottom of this page. Once you have completed the course, please complete and submit the Course Evaluation form (there is also a link at the bottom of the course main page).

This course provides introductory training on the Adulterated Product Monitoring (APM) functionality of the Public Health Information System (PHIS), which is used to document industry notification that an establishment has received or shipped adulterated product that is in commerce. Previously, only OIEA and OFO District Office personnel have used APM for reporting. However, this course is designed for in-plant CSIs and PHVs who may now also have a role in APM reporting. This training focuses on how to utilize the APM functionality in PHIS as outlined in FSIS Directive 8140.1, Revision 2. It covers background on the requirements for reporting the receipt or shipment of adulterated product, the active PHIS reporting tools, how Draft Reports are initiated, and the information IPP will enter to contribute to reports.

*Disclaimer: The scenarios/examples used are for training purposes only and do not represent real incidents of receipt or shipment of adulterated or misbranded product.

Technical Support: Email CFLHelpDesk@usda.gov or call 1-833-ASK-OEED (1-833-275-6333), Mon-Fri - 8:00am - 5:00pm ET for assistance. Do not contact the FSIS FootPrints Service Desk if you need assistance with this training system.
- Select activity How to Use Interactive Features
  
  How to Use Interactive Features Interactive Content
Select section APM Presentation

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APM Presentation
- Select activity APM Lesson #1 Adulterated Product Module Introduction & Regulatory References
  
  APM Lesson #1 Adulterated Product Module Introduction & Regulatory References Interactive Content
Select section Regulatory Overview

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Regulatory Overview
- Select activity APM Lesson #2 APM Tool Overview
  
  APM Lesson #2 APM Tool Overview Interactive Content
- Select activity APM Lesson #3 Overview of IPP Responsibilities
  
  APM Lesson #3 Overview of IPP Responsibilities Interactive Content
- Select activity APM Lesson #4 IPP Responsibilities at Receiving Establishment
  
  APM Lesson #4 IPP Responsibilities at Receiving Establishment Interactive Content
- Select activity APM Lesson #5 Creating the IRA-IP in PHIS at the Receiving Establishment
  
  APM Lesson #5 Creating the IRA-IP in PHIS at the Receiving Establishment Interactive Content
- Select activity APM Lesson #6 IPP Responsibilities at the Shipping Establishment
  
  APM Lesson #6 IPP Responsibilities at the Shipping Establishment Interactive Content
- Select activity APM Lesson #7 Final Summary of the APM PHIS Tasks and Course Survey
  
  APM Lesson #7 Final Summary of the APM PHIS Tasks and Course Survey Interactive Content
Select section APM Resources

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APM Resources
- Select activity Simulation - Close IRA-IP Case
  
  Simulation - Close IRA-IP Case URL
- Select activity Simulation - Create IRA-IP Case
  
  Simulation - Create IRA-IP Case URL
- Select activity SImulation - Update IRA Case
  
  SImulation - Update IRA Case URL
- Select activity Directives
  
  Directives Folder
- Select activity Regulations
  
  Regulations Folder
Select section Course Evaluation

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Course Evaluation
Please follow the link to complete and submit a short Course Evaluation form. The responses and comments you provide will help us to continually improve the virtual learning experience.