My Audit Corner Webinars
Expert exchanges, live demonstrations, and regulatory insights for Medtech RA/QA professionals.
Upcoming
Two people on the team, an entire portfolio to cover: what if Medtech compliance became manageable?
ISO 13485, MDR, IVDR. Three frameworks, dozens of technical files, periodic reviews, internal audits. And often, just two or three people to manage it all.
If you lead or oversee a Medtech team, these questions probably resonate:
- How can you know, at any moment, the real compliance status of your entire portfolio?
- How do you move from reactive compliance to continuous, monitored compliance, without hiring?
- How do you give your quality team the means to keep up the pace, without multiplying tools or providers?
Program
Sébastien Risler (CEO, My Audit Corner)
Live platform demo: continuous compliance assessment of your QMS and technical files, automated prioritization and roadmap, actionable plan, team task management, internal audit, integrated chat, regulatory monitoring, supplier management, and PRRC dashboard.
Charles Rollet (CEO, TraceX)
Overview of the TraceX platform and its integration with My Audit Corner to complete your compliance value chain.
For: executives and quality leaders of Medtech SMBs and scale-ups who want to structure their compliance day to day, not only when an audit is approaching.
By the end of this webinar, you will have a clear view of how these tools fit into your routine to secure ISO 13485, MDR and IVDR compliance, without multiplying resources.
Replays
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MDD to MDR Transition: Secure Your Technical File and Accelerate Compliance with AI
The MDD to MDR transition is a major strategic challenge. This webinar brings together a regulatory expert and a cybersecurity specialist to present concrete solutions combining technological performance and information security: automated status assessment, prioritized action plans, secure hosting, and real-world use cases.
Desk evaluation and GSPR
The shift from on-site audits to remote evaluation: why the GSPR matrix is the gateway to your technical documentation.
Structuring technical documentation
Searchable PDFs, preliminary review, self-contained sections: keys to facilitating the evaluator's work and avoiding non-conformities.
Cybersecurity and risk sources
AI-powered targeted phishing, external exposure, supply chain: mapping the main threats to your regulatory data.
SaaS security best practices
Least privilege, data segregation, encryption, two-factor authentication: essential practices to protect your data in cloud environments.
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AI Serving Internal Audits: What Changes Concretely for RA/QA Teams
This webinar explores artificial intelligence's impact on internal audits in the Medtech sector, focusing on quality management systems (ISO 13485) and associated operational challenges.
The Notified Body Perspective
Acceptability of AI-generated reports, AI Act impact, and real-world regulatory expectations.
AI Technology Reality
Generic AI limitations (hallucinations, volume issues), and benefits of RAG and agent orchestration.
Business Knowledge Digitalization
How Multi-Agent architecture analyzes your data with auditor-level rigor.
Live practical case
Demonstration of automated, reliable, sourced internal audit generation in My Audit Corner.