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Our experts are here to help you achieve your goals. They share valuable insights on many different topics in our webinars. Find your know-how!

  • July 12, 2021

    Webinar In-Vitro Diagnostics Regulation (IVDR)

    DEKRA Certification B.V. is now recognized as a Notified Body by the European Commission under the new EU regulation on in-vitro diagnostics (IVDR 2017/746). Under the new regulation, considerably stricter requirements will apply to manufacturers of in-vitro diagnostics (IVDs) in the European Union. During this webinar we discuss the most relevant topics related to the new IVDR.

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    June 10, 2021
    Webinar ESS

    Webinar Energy Storage Systems (IEC 62933-5-2:2020)

    During this webinar IEC 62933-5-2:2020 will be presented by our Industrial Safety team, from an entry level approach. It will highlight the key technical aspects, such as testing requirements and the process towards certification.

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  • November 11, 2020
    IECE 60601 webinar

    IEC 60601-1

    The IEC 60601-1 standard applies to the basic safety and essential performance of all medical equipment and medical electrical systems. The standard gives guidance for safety from unacceptable risk under normal condition and single fault condition of electrical, mechanical and other hazards.

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    November 4, 2020
    NRTL webinar

    DEKRA North American Certification Scheme

    DEKRA has established its own North American Certification Scheme (NACS) and is an accredited assessment body for both the US and Canada. DEKRA already has decades of expertise in the North American certification market via a network of accredited partners.

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    Cybersecurity on Consumer IoT devices

    The consumer IoT ecosystem is growing at a fast pace, and with it, the security requirements and regulations affecting these devices. Manufacturers need to prepare their products to assure users' safety as well as the security of the devices. We invite you to watch this on-demand webinar to learn about this topic!

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  • January 23, 2018
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    MDR Classification and Conformity Assessment Routes

    The third webinar in the MDR expert series focuses on the changes in Classification and Conformity Assessment Routes in the MDR compared to the Medical Device Directive (MDD).

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    February 15, 2018
    Blood Vials

    IVDR: Status & Highlights

    In this status update we talk a.o. about:

    • An overview of the differences between IVDD and  IVDR
    • The classification system of the IVDR
    • The conformity assessment IVD


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    April 26, 2018
    IEC 60079-0

    New Edition 7.0 of IEC 60079-0

    IEC 60079-0 contains the basic requirements for all electrical products that need to be certified for use in zone classified areas and is therefore mandatory.


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  • 23 October 2017
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    MDR Status & Highlights

    In this status update we talk a.o. about:

    • Timelines of the transitional period
    • Impact on CE certificates
    • Validity MDD and AIMDD certificates
    • Transitional provisions

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    November 30, 2017
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    New edition 7.0 of IEC 60079-0

    In this status update we talk a.o. about:

    • Preview into first changes of new standard
    • How you can start preparing


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    19 December 2017
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    MDR Clinical Evaluation Requirements

    DEKRA's experts address, amongst others:

    • Clinical evaluation
    • Post market surveillance and pm clinical follow-up
    • CE mark obtained through equivalence

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  • October 25, 2016
    Image webinar

    How the introduction of the new MDR and IVDR will impact you

    In this status update we talk a.o. about:

    • How can you prepare for the changes?
    • How will they impact your organization?
    • What are the most important highlights?


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    December 6, 2016
    Image webinar

    Webinar upcoming change: transition to MDSAP

    In this status update we talk a.o. about:

    • How can you prepare for the changes?
    • How will they impact your organization?
    • What should I do to become MDSAP certified?


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    September 12, 2017
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    Unlocking opportunities in the GCC markets

    In this status update we talk a.o. about:

    • Gulf Cooperation Countries in the GCC markets
    • Scope and upcoming changes
    • Technical documentation requirements
    • Registration system GSO

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  • April 7, 2016
    Image webinar

    New EMC Directive 2014/30/EU

    In this status update we talk a.o. about:

    • Changes from the previous directive
    • The role of NBs and economic operators
    • Requirements on marking and technical documentation
    • Updates on harmonized standards

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    May 31, 2016
    Image webinar

    ISO 13485:2016

    In this status update we talk a.o. about:

    • How the transition will impact you
    • In combination with transition ISO 9001:2008 to ISO 9001:2015


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    June 2, 2016
    Image webinar

    IEC 62368: the new safety standard

    In this status update we talk a.o. about:

    • The basics
    • The objectives
    • Products covered by the standard
    • Practical information

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