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TÜV Open Day Seminars

  

Please click on the seminar titles below to download the seminar material.

11:15 - 12:00 - Testing active medical devices - new challenges [ PDF 335 kB ]

G1A - Presented by Norman Richardson

New and recently updated collateral standards. How your risk management file also needs to cover the requirements of the IEC 60601-1 3rd Edition. Implementation dates and related considerations. New symbols in EN 9802008.

11:15 - 12:00 - R&TTE directive: How to place your transmitting devices on the market in the EU [ PDF 682 kB ]

G1B - Presented by Michael Lowry

An insight into the R&TTE directive from a manufacturer's point of view.

11:15 - 12:00 - The New EMC Directive – 2004/108/EC [ PDF 2115 kB ]

Customer Rm - Presented by Damon High

2004/108/EC came into force July 2007 with a 2-year transition until July 2009. The requirements for apparatus and trains has changed and there are new requirements for fixed installations.

1:15 - 14:00 - Electrical Safety Compliance Made Easy [ PDF 879 kB ]

G1A - Presented by Mark Penton

A practical approach guide to what you need to know when submitting products for electrical safety testing.

1:15 - 14:00 - Environmental Testing: To test or not to test? [ PDF 814 kB ]

G1B - Presented by Richard Thompson

Look at how requirements flow from the end customer through to the test programme and how testing can be kept to a minimum, thereby reducing costs and time for the programme whilst maintaining its integrity.

1:15 - 14:00 - We bring it closer to you, EMC testing with remote monitoring [ PDF 494 kB ] [ PDF 494 kB ]

Customer Rm - Presented by Prabhu Ramkumar

Our customers can now monitor their test programmes online, saving time and reducing travel cost. Learn more how this service can benefit you with a hands on demonstration.

14:00 - 14:45 - Highly Accelerated Life Testing (HALT): Helping you to reduce time to market and improve cost efficiency

HALT Lab - Presented by Chris Bowles

Like to know more about HALT? This Seminar will allow you to understand the methodology and how this can benefit your products.

14:00 - 14:45 - An overview of SAR for transmitting devices used near the human body

SAR Lab - Presented by Alex Miller

With the ever increasing use of radio transmitting devices used in consumer electronics, it is important to ensure that manufacturers consider the effect this may have on the user. SAR (Specific absorption rate) evaluation is essential for any transmitting device that is used in close proximity to the human body. It is becoming more and more important as the trend towards wireless products increases and is an essential requirement for anyone placing such products on the worldwide market.

15:00 - 15:45 - REACH: What is it and how does it affect you? [ PDF 1027 kB ]

G1A - Presented by Markus Jahns

The REACH (Registration, Evaluation and Authorisation of Chemicals) regulation is now in force, and it’s important that all manufacturers, importers and downstream users of chemicals are prepared, and fully aware of the impact this new legislation has on their business.

15:00 - 15:45 - Upcoming changes to the Medical devices directive [ PDF 489 kB ]

G1B - Presented by Henry Sibun

The changing directives in the Medical device market, are you prepared ?

15:00 - 15:45 - Lightning testing: Overview and demonstration [ PDF 696 kB ]

Lightning Lab - Presented by Chris Bennett

Guidance on the latest lightning test requirements and a practical demonstration of testing.


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