Mastering Global Supply Chain Dynamics with Unparalleled Quality Practices
In today’s global clinical trial environment, orchestrating a seamless supply chain involves far more than moving products from point A to point B. From sourcing and manufacturing to labeling, distribution, and returns, each step demands meticulous oversight to prevent costly interruptions and maintain compliance.
Within this larger ecosystem, the Qualified Person (QP) serves as a critical checkpoint, certifying every batch against Good Manufacturing Practice (GMP) standards and safeguarding both patient safety and trial integrity.
Join our interactive panel discussion to hear industry experts share how implementing quality assurance and quality control measures can mitigate risks and ensure compliance with regulatory standards.
Learning Objectives:
- Pinpointing strategies to boost quality at each stage — from production to trial-site delivery
- Practical insights on aligning trial logistics with shifting global regulations
- Providing thorough QP oversight to ensure every product meets strict quality and regulatory standards
Speakers:
- Yuyi Shen, Vice President, Technical Operations, Abcuro
- Michelle York Gocio, Vice President, Drug Development and Clinical Operations, Novatek Pharmaceuticals
- Marian Kulich, VP Clinical Supply Chain Operations, SanaClis
- Sascha Sonnenberg, VP Global Business Development & Country Head Germany, SanaClis
