Free Live Webinar: Automating Medical Devices QA Process with Agentic AI Reserve your Seat Now!
LIVE WEBINAR

The AI-Powered Quality Team
Automating Medical Devices QA Process with Agentic AI

This session is for you if any of this sounds familiar.

  • Your QA team is drowning in manual, repetitive documentation work.
  • You have tried generic AI tools like ChatGPT, but they take more time in prompting than they give back in real automation.
  • You do not know what a real, working AI automation setup actually looks like for QA.
Thu, Oct 01, 2026
11:00 AM ET
45 min + Live Q&A
Online

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    Why Attend

    Outcomes you can take back to your team

    A clear framework for evaluating where AI automation fits in your QMS

    You will walk away knowing which QA processes, such as CAPA or complaints, are the best candidates for automation, and which still need human judgment.

    A checklist for spotting when generic AI tools are a compliance risk

    Practical criteria you can use to evaluate any AI tool your team is considering, before it creates an audit liability.

    A real reference example to bring into your next quality or leadership meeting

    A concrete, working demo you saw firsthand, not a theoretical pitch, that you can use to start the automation conversation internally.

    The confidence to be the one who introduces this to your organization

    You will leave able to explain, demo, and defend the idea of agentic AI in QA to skeptical colleagues or leadership, not just describe it secondhand.

    Whether you own full QA responsibility or a specific area such as CAPA, Complaint Handling and Post-Market Surveillance, or Audits and Inspections, this session gives you a practical way to identify where AI fits, what to automate first, and how to introduce it with the right human oversight and governance.

    Agenda

    45 minutes, straight to what matters

    01

    Where AI fits inside a validated quality system, and where it does not

    02

    Which MedTech Quality workflows are most ready for AI automation

    03

    What your quality data and QMS need before you automate

    04

    Validation, human oversight, and audit trails in practice

    05

    Live Q&A

    Who Should Attend

    Built for MedTech quality leaders

    Quality and Compliance Leadership

    • Quality Assurance
    • Quality Operations
    • QMS
    • Quality Compliance
    • Quality Systems
    • Quality Engineering

    Quality Processes You Own

    • Design Controls and Risk Management
    • Documentation and Records Management
    • CAPA and Nonconformance Management
    • Audits and Inspections
    • Verification and Validation
    • Complaint Handling and Post-Market Surveillance
    Written for Manager level and above, including Directors, Heads and VPs who own quality systems and their outcomes.

    Abarna Sakkaraipandi

    Quality & Regulatory Specialist | ISO 13485 Lead Auditor, Dash Technologies

    Quality and regulatory professional focused on ISO 13485 compliance, QMS implementation, and audit ready medical device processes. Abarna works daily in the QA processes this session automates, from CAPA and nonconformance through documentation, records, and audit preparation, and brings QMS expertise that reaches beyond device QA. She will lead the session and run the Q&A.

    • Healthcare and MedTech engineering practice at Dash Technologies
    • Hands on AI implementation across regulated healthcare workflows
    • Quality and regulatory expertise for MedTech environments, from QMS to audit readiness
    • OpenAI Select Partner