Speaker Biography:
Richard Tully is a medical device regulatory leader with 15+ years of global experience, including serving as Special Advisor on Medical Devices to the Saudi FDA and supporting compliance across the EU, UK, and Africa.
Outlines:
- Process-based systems overview
- Writing effective procedures
- Clause-by-clause QMS requirements
- Internal auditing
- Corrective & Preventive Actions (CAPA)
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