February 26, 2026
The qualification of suppliers in accordance with Good Distribution Practices (GDP) and Good Manufacturing Practices (GMP) is a legal obligation for pharmaceutical companies and requires the proper qualification of their internal resources. A thorough understanding and evaluation of pharmaceutical supply chains, including finished products and raw materials, is essential to ensure product quality, safety, and regulatory compliance.
Establishing robust systems to manage supplier qualification is therefore critical. However, these systems must also be designed to remain agile and efficient, minimizing process timelines while maintaining full compliance with regulatory requirements.
• Understand the main guidelines and standards related to the qualification of suppliers;
• Understand the expectations of customers and authorities regarding this topic;
• Learn the basics of designing effective and compliant supplier qualification systems.
1. Applicable guidelines and standards;
2. Importance of Supplier Qualification;
3. Supplier’s Qualification process:
a. Identification and Selection criteria for different types of suppliers
b. Evaluation
c. Monitoring
4. Supplier’s Qualification and Risk Management;
5. Reduced testing;
6. Challenges and improvements;
7. Inspector expectations;
8. Case studies and discussion.
You will receive an email confirming availability and providing payment details. Registration will only be considered complete upon confirmation of payment.
200 € + VAT
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