Free Live Webinar,
GxP

Everything You Need to Know About Risk Management (ISO 14971)

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Date

Dec 17 2025

5:00 PM – 6:30 PM, Central European Time (CET)
11:00 AM – 12:30 AM, Eastern Time (ET)
Time

Overview

Are you confident your medical device risk management processes meet the ISO 14971 standard?

ISO 14971 provides a detailed blueprint for managing risks effectively throughout your medical device’s lifecycle — a key factor for regulatory approval and successful market entry.

Join our expert-led webinar to:

  • Understand what ISO 14971 risk management looks like in practice for your medical device company.
  • Learn how to implement best practices that ensure robust and compliant risk management.
  • Discover top tips for controlling your medical device risks and driving a right-first-time approach to market.

Don’t miss this opportunity to strengthen your risk management system and ensure safer products for patients and users.

Register now to reserve your spot!

Speaker

  • Lola Furlong
    Lola Furlong
    Senior Quality Success Manager, Qualio

    Lola is an ASQ Certified Medical Device Auditor with extensive experience at large multinational corporations and start-ups across Europe and North America.

    She works closely with Qualio customers to implement and maintain their eQMS, helping them to achieve their quality and risk management goals and bring their medical devices to market efficiently.

Partner

Qualio
Qualio
Website
https://qualio.com/

Founded in 2012, Qualio is the first cloud quality management software for all Life Sciences companies. Medical device and pharmaceutical companies need a secure and scalable quality management system with the flexibility to support their evolving needs. Qualio meets that challenge by cutting through the complexity to optimize and automate critical quality processes. The remote-first, Qualio team is distributed across North America and Europe.

  • Who Should Attend
    • Pharmaceutical quality
    • Compliance professionals
    • Risk professionals
  • Skill Level Novice
  • Topics
    • Understanding of ISO 14971 requirements and how to embed them.
    • How to get best-in-class device risk management in place using the internationally recognised ISO 14971 framework.
    • Get a demo of a Compliance Intelligence AI tool and its ICH Q10 framework.
  • Special event information

    Participants will recieve a certificate of attendance.

Date

Dec 17 2025

Time
5:00 PM – 6:30 PM, Central European Time (CET)
11:00 AM – 12:30 AM, Eastern Time (ET)

  • 00

    days

  • 00

    hours

  • 00

    minutes

  • 00

    seconds

Speaker

  • Lola Furlong
    Lola Furlong
    Senior Quality Success Manager, Qualio

    Lola is an ASQ Certified Medical Device Auditor with extensive experience at large multinational corporations and start-ups across Europe and North America.

    She works closely with Qualio customers to implement and maintain their eQMS, helping them to achieve their quality and risk management goals and bring their medical devices to market efficiently.

Partner

Qualio
Qualio
Website
https://qualio.com/

Founded in 2012, Qualio is the first cloud quality management software for all Life Sciences companies. Medical device and pharmaceutical companies need a secure and scalable quality management system with the flexibility to support their evolving needs. Qualio meets that challenge by cutting through the complexity to optimize and automate critical quality processes. The remote-first, Qualio team is distributed across North America and Europe.

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