With persistently changing regulatory requirements both domestically and internationally, medical device companies worldwide have struggled to ensure that consumers receive high quality products. Managing quality events within the quality system and throughout the supply chain are seminal in uncovering the source of what ultimately determines the quality, safety, and efficacy of products.
The workshop and seminar Master Control: Integrating Risk-based Supplier Auditing (RSA) into Your Quality System, will provide you with information on critical supply chain sourcing, help you understand the role that quality and compliance auditing plays in successful supplier management, and inform you on how to use a risk-based approach to prioritize and escalate the control of events, including corrective and preventive actions (CAPA). In a business climate where outsourcing is becoming the norm, RSA is critical to developing a compliant quality system.
MasterControl Insights: May 7, 8:45 to 17:00 in Zurich (Zunfthaus zur Saffran, Limmatquai 54, 8001 Zürich).
- Understand supplier management, control and the risk-based approach
- Employ best practice preventive controls through supplier evaluation
- Know the intent and application of regulatory guidance and expectations
- Implement monitoring and improvement actions effectively
Spaces for the MasterControl seminar are limited and will be filled on a first come first served basis. For more information and to register, please register here.
Organisation Sarah Moyle, Head of International Relations Medtech Switzerland Tel. +41 31 335 62 41 [email protected] www.medtech-switzerland.com
