Join our team of experts as we explore the extensive capabilities of D365 with Alithya 365 Enhanced Quality and Compliance, providing your medical device organization with the tools and insights necessary for achieving not only swift market entry but also elevated levels of quality and compliance. This webinar caters specifically to professionals in the medical device industry who are looking to implement D365, ensuring a more efficient and compliant operational environment. Seize this chance to stay at the forefront of advancements in business technology within the dynamic landscape of the medical device sector.
Key Learning points:
Elevating Electronic Signature Processes:
Support for 21 CFR Part 11 required E-Signatures.
Navigating Non-Conformance Records (NCR):
Exploration of how D365 can be harnessed to effectively manage Non-Conformance Records (NCR) in the medical device industry, minimizing risks and ensuring timely resolution.
Comprehensive CAPA Management:
Understanding the integration of Corrective and Preventive Actions (CAPA) within the D365 framework tailored for medical devices, promoting a systematic approach to issue resolution.
Unlocking Rapid Entry for Quality Management Through D365:
How to utilize quality management for quick results entry to ensure agility without compromising accuracy.
Seamless Lot Tracing with Device History Records:
Demonstrating how D365 facilitates efficient lot tracing through enhancing traceability and accountability in the context of medical devices.
Implementing the D365 Platform and the FDA Validation Process:
Insights into the additional milestones when deploying D365 in FDA validated environment.
Live Demonstration:
A hands-on demonstration showcasing examples of practical implementation of the discussed strategies within the D365 environment, emphasizing their relevance to medical device operations.
Speakers:
Traci Didonna, Principal Program Manager, Alithya
Juan Aguilar, Supply Chain Technical Specialist, Microsoft
Michael AuBuchon, Account Executive, Alithya
