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Mastering ISO 13485 Compliance for Medical Device Companies

Language : English

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Apr 30 , 2025, 11:00- UTC-04:00 ^?

Online
Free of charge

Online

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Key Aspects: Purchasing Control, CAPA, and Complaint Management of ISO 13485

In cooperation with RQM+, DQS is running an expert-led webinar designed specifically for medical device companies. We will share what you need to navigate and implement ISO 13485 standards effectively in your organization.

This session will cover:

Purchasing Control: Best practices for maintaining control over suppliers and ensuring the quality of purchased materials.
CAPA (Corrective and Preventive Actions): Learn how to develop and implement effective CAPA systems to address non-conformities.
Complaint Management: Understand how to effectively handle and resolve customer complaints in compliance with ISO 13485.

Expert speakers on ISO 13485:

Claire Dyson – Managing Director, DQS Medizinprodukte UK (Notified Body)

Richard Freeman – Director, Global Audit Practice at RQM+

Rem Siekmann – Senior Principal Engineer at RQM+

Gain actionable insights from industry experts, learn how to avoid common pitfalls, and ensure your organization meets regulatory requirements.

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Session details:

When: April 30, 2025, 11:00 AM EST
Duration: 1 Hour including Q&A time
Delivery: Online
April 30, 2025 Free of charge

Who is this for?

Professionals in the medical device industry, including regulatory affairs specialists, quality assurance teams, manufacturers, startups, consultants, and legal experts aiming to navigate FDA and MDR approval processes.

Prerequisites

No prior expertise required or basic knowledge of medical device regulations.
Ideal for anyone interested in understanding the ISO 13485 approval processes, from beginners to industry professionals.
Suitable for all roles in the medical device sector.

By the end of this ISO 13485 webinar, you will have mastered:

Purchasing control for Medical Device companies

Best practices for maintaining control over suppliers and ensuring the quality of purchased materials.

CAPA for non-conformities

How to develop and implement effective Corrective and Preventive Actions (CAPA) systems to address non-conformities.

Advanced complaint management

Understand how to effectively handle and resolve customer complaints in compliance with ISO 13485.