Supplier & Contract Manufacturer Management Online Training Course: Ensure Compliance, Reduce Risk & Improve Supplier Performance (ON-DEMAND)

Dublin, May 21, 2026 (GLOBE NEWSWIRE) -- The "Supplier & Contract Manufacturer Management: Ensure Compliance, Reduce Risk & Improve Supplier Performance (May 18th - May 19th, 2026)" training has been added to ResearchAndMarkets.com's offering.

This training provides a practical, lifecycle-based approach to supplier management - from qualification and risk assessment to performance monitoring, auditing, and supplier transitions.

This course is a must for anyone looking to strengthen supplier relationships, enhance contract manufacturer oversight, and ensure regulatory and quality compliance throughout the manufacturing process.

What's Included:

Suppliers and contract manufacturers play a critical role in product quality, regulatory compliance, and supply chain reliability.

Poor supplier oversight can lead to quality failures, audit findings, supply disruptions, and increased costs.

By attending this training, you will be able to:

Why this training is important:

Business impact of poor supplier management:

You will build during this training:

Who Should Attend:

Key Topics Covered:

Strategy, Risk & Supplier Qualification

Session 1: Foundations of Supplier Management

Session 2: Regulatory Requirements & Business Impact

Session 3: Strategic Supplier Management

Session 4: Risk-Based Supplier Qualification

Agreements, Performance & Audits

Session 5: Supplier Relationships & Quality Agreements

Session 6: Performance Monitoring & Improvement

Session 7: Supplier Assessments & Audits

Session 8: Supplier Lifecycle & Transitions

Speakers:

Kelly Thomas

Vice President

Stallergenes Greer

Ms. Thomas 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.

For more information about this training visit https://www.researchandmarkets.com/r/y9xiw4

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