Establishing a Robust Supplier Management Program

Establishing a Robust Supplier Management Program


  Vice President

Stallergenes Greer

  Product ID : HOMA-0009

  Level : Intermediate

  Duration : 90 Minutes

Ms. Thomas, Vice President, Americas Quality Operations at Stallergenes Greer and has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations. Her experience covers all Quality Systems; as well as, all areas of validation; including, process/product validation, facilities validation, CSV and 21 CFR Part 11, test method validation, equipment/automated processes, and cleaning validation.

Utilizing strategic thinking, risk-based approaches, and Lean principles, she has demonstrated success in steering and managing complex projects within the pharmaceutical and medical device industries.

Regulatory expectations are clear about manufactures’ responsibility regarding supplier quality oversight. All regulatory agencies agree that pharmaceutical and medical device manufacturers are responsible for ensuring their suppliers adhere to quality standards, maintain compliance with regulatory requirements and consistently meet established expectations. Therefore, it is essential pharmaceutical and medical device organizations develop and implements a robust supplier management program.

A robust program is one that utilizes a comprehensive life-cycle approach that manages suppliers from initial qualification through phase-out. In other words, from cradle to grave. A robust, yet efficient, supplier management program is one that also utilizes a risk-based methodology to determine supplier criticality and the required level of oversight.

This course will review regulatory guidance governing Suppliers; as well as, all the elements of a robust supplier management program; including, initial qualification, supplier performance monitoring and scorecards, supplier audit options, and quality agreement requirements. An example Supplier Management Standard Operating Procedure (SOP) and Quality Agreement template will be reviewed during the course.

This course will also include a discussion on how to utilize risk-based quality tools to determine supplier classification. An example supplier risk assessment will be reviewed during the course. Finally, in order to understand the real-life consequences associated with non-compliant supplier management programs, recent FDA audit findings will be reviewed and discussed.

Areas Covered    

I. Review Supplier Management Regulatory Guidance

  • ISO
  • ICH
  • FDA
  • EU

II. Elements of a Robust Supplier Management Program

  • Standard Operating Procedure (SOP) example
  • Quality Agreement template review
  • Initial qualification
  • Onboarding
  • Monitoring / Scorecards
  • Development
  • Phase-Out

III. Review of Risk Analysis Tools and Recent Audit Observations

  • Review an example FMEA classifying different suppliers by criticality
  • Review recent FDA audit observations applicable to supplier management

Course Level - Fundamental or Intermediate

Who Should Attend

  • QA Managers and Associates responsible for supplier management
  • Supply Chain Managers and Associates
  • Operations Managers
  • Managers and QA personnel from Contract Manufacturing Organizations (CMOs)
  • Regulatory and quality professionals working for US companies that are considering foreign suppliers
  • Suppliers outside the US looking to US-based clients
  • QA/QC/Compliance/Regulatory affairs professionals
  • $200.00

Recorded / Download Access