Medilink WM and MasterControl invite you to attend a free workshop to learn more about the changing medical device regulatory environments, successfully navigating audits and the value of using digital solutions for managing quality and compliance. Offering attendees a better understanding of ‘How to be nimble in an ever-changing regulatory environment and easily manage the audit process with digitisation.’
Highly-knowledgeable life sciences industry experts will provide valuable insight on these topics and demonstrate how medical device and component manufacturers can position themselves for success.
You will hear from industry experts including Stephen Turnock, Global Sales Director EMEA, MasterControl and guest speaker Matthew Theobald, Three Circles who will cover:
- Medical Device Audit Fundamentals, MD SAP including the regulatory impact on audits
- Assessing your company’s current readiness for implementing a quality platform, (MasterControl EBR)
- An overview of the regulatory and quality management system requirements for a concept medical device, understand the technical document that should be in place and explore risk management.
- Improve Product Quality & Operational Efficiency with Paperless Processes
Attendees also have the opportunity to a private tour of the MTC facility.
This workshop will include opportunities to network and learn from your peers about their best practices and use of technology to navigate regulatory pathways and achieve compliance.