Recorded Webinars

This webinar is recorded by DQS to provide an overview of the key changes in the upcoming ISO 14001:2026 revision and actionable strategies to successfully prepare your Environmental Management System (EMS).

Webinar Topics:

1. ISO 14001:2026 vs. ISO 14001:2015: A structured comparison of key changes and updated requirements.
2. Transition Planning: Practical roadmap and actionable steps to prepare your EMS for certification upgrade.
3. Key Audit Impacts: Understanding how the updates affect your environmental policies and compliance.
4. Expert Guidance: Insights and practical Q&A with environmental management expert Ron Leung.

Get the full presentation slides from our ISO 14001:2026 revision webinar for a detailed, step-by-step guide to preparing your EMS.

What's inside:

1. Executive summary of ISO 14001 updates
2. Practical transition roadmap & timeline
3. Expert insights by Ron Leung

This webinar is recorded by DQS Inc and to provide an overview of the changes ISO 27001:2022 and ISO 27002:2022, as well as the timeline for certification upgrade.  

This webinar is recorded by DQS Inc and aimed at providing you an overview of "A Day in the Life of an ISMS Audit," from a high-level look at a typical agenda through an ISO 27001 Audit path that provides examples of the approach you can expect to test your management system.

This webinar is recorded by DQS Inc and aimed to provide you an overview of “TISAX® – Why and What”. The Why – focuses on not only information security but also the OEM needs based on what product and/or services that you provide. While the What covers the aspects of ISO 27001 and other key standards and discuss the audit process and model.

Webinar Topics:

• Understand the TISAX® VDA ISA Model 5.0.4 including catalog items and maturity level
• Overview of the TISAX® Audit Process
• Summary of the TISAX® Materials Available on the ENX Website
• Keys to getting started with TISAX®

This webinar is recorded by DQS Inc and aimed at providing you an introduction to the Medical Device Single Audit Program. It covers the benefits of MDSAP certification and highlight the additional requirements beyond ISO 13485:2016. Participants will learn tips for preparation, answers to frequently asked questions and gain an understanding of the application and audit process.

MDSAP is designed to harmonize Medical Device Manufactures’ Management System Certification using a Single Audit Program. MDSAP with ISO 13485:2016 is required if you provide medical devices into Canada and can streamline the regulatory application process for medical devices provided into Australia, Brazil, Japan, and the United States.

DQS offers the MDSAP service through authorizations and oversight by DQS Medizinprodukte GmbH which is a MDSAP Recognized Auditing Organization. Please join us for a webinar presented by Marc Goedecke who heads our MDSAP program at DQS MED.

The new Regulation (EU) 2017/745, called MDR was published on May 5, 2017 and entered into force on May 25, 2021. Therefore, the new Regulation (MDR) replaces the previous Medical Device Directive MDD 93/42/EEC and the Active Implantable Medical Devices Directive AIMD 90/385/EEC.

This webinar, presented by Andreas Geringer, will give you a brief introduction into the procedures and possible obstacles on the way to the certification.