Webinars

FREE Webinars at the touch of a buttonwebinars.jpg

TÜV Product Service is launching a new
programme of webinars.

Webinars are a new medium that allow presentations and training to be communicated over the web. It is very simple for you to enjoy the benefits as all you will need to view and hear our webinars is internet access and a sound-enabled PC. And our webinars are free and will take no longer than 60 minutes!

Our webinars will be presented by TÜV SÜD Product Service experts, providing you with up to the minute information that affect you as compliance professionals along with the opportunity to interact from the convenience of your office or home.

Now you have the option to view pre-recorded webinars, all you need is a computer with a high-speed internet connection and speakers to view our webinars anytime, for free. CLICK HERE
 

Webinars Throughout 2010

Importing Products for Retail 

Wednesday 31st March 2010 at 2:00pm

Overview of presentation
This presentation looks at the issues facing retailers importing product manufactured outside the EU when placing them onto the market, including the legal obligations and responsibilities. It reviews the lifecycle of a retail product and the steps that can be taken during this to ensure that product issues such as complaints & returns are minimised. The aim being to help you protect yourself and minimise the risks when importing products.		 

Who should attend
This Webinar is aimed at anyone importing products with the intention of placing them on the European market.

 

Benefits for attending the webinar
This webinar will give guidance to help you understand the issues facing anyone importing product into the EU marketplace and what steps can be taken to help protect yourself and your consumers.

 

CLICK HERE TO BOOK YOUR SPACE NOW

CE Marking and your legal obligations

 Wednesday 28th April 2010 at 2:00pm
More Info to follow shortly More Info to follow shortly
An Introduction to the British Retail Consortium Consumer Products Scheme Wednesday 26th May 2010 at 2:00pm

Overview of presentation

This webinar is intended to introduce the British Retail Consortium (BRC) Global Standard for Consumer Products Certification Scheme and familiarize attendees with the requirements of Issue 3 of the Consumer Products Standard.  This webinar will be a general familiarization session suitable for retailers, distributors and certification staff.

 

Who Should Attend

The course is suitable for compliance engineers, auditors, test engineers and marketing and sales staff seeking to gain knowledge of the BRC Consumer Products Scheme.

 

Benefits of attending

People attending this course will benefit from a clear presentation of the newly introduced Issue 3 of the BRC Consumer Products Standard, its requirements and objectives for bringing to the market products that are safe, legal and fit for purpose.

New requirements for electro-medical devices, 60601-1 3rd Edition Wednesday 30th June 2010 at 2:00pm

Overview of presentation
The requirements for the basic safety of medical electrical equipment, IEC 60601-1, have moved a long way since the first edition in 1978.  The 2005/6 edition, referred to as the 3rd Edition, incorporates many concepts new to this standard.  Examples are: greatly raised profile of risk assessment and management, new leakage current concepts and mechanical hazards covered to a much greater extent and in more detail than before.  Manufacturers have only until June 2012 to move to this standard after which the 2nd Edition will be withdrawn and with it the presumption of conformity to the relevant requirements of the directives to which it is harmonised.

 

Who should attend
Manufacturers, repairers and refurbishers of medical electrical equipment.

 

Benefits for attending

This webinar will give guidance to help you understand the major changes.  It will highlight the key issues for your design, test and regulatory affairs departments and assist you in making trouble-free submissions to a test house.
Environmental Testing Wednesday 14th July 2010 at 2:00pm
More Info to follow shortly More Info to follow shortly
EMC - Fundamentals of Design & Testing Wednesday 29th September 2010 at 2:00pm
More Info to follow shortly 

More Info to follow shortly

Updates on FCC Certification Procedures and Requirements Wednesday 27th October 2010 at 2:00pm

Overview of presentation
This webinar will present the latest updates on FCC rules, regulations and policies to give you a better understanding of the latest processes and procedures for gaining FCC approvals in the US. The training will feature critical technical updates on regulations and policies from the FCC/TCB Council training in October 2010.

 

Who should attend
The FCC Regulations have implications for suppliers of all radio apparatus intending to place product on the US market. The presentation would increase understanding of the FCC Regulations for Compliance/Project Managers as well as Test Engineers and Technicians conducting Testing to US requirements.  Design and Development engineers and technicians may benefit from receiving the latest updates.

 

Benefits for attending

This webinar will give guidance to help you understand new FCC requirements and changes to FCC Regulations and will enable you to gain maximum benefits in your compliance strategy.
Sterilization of Medical Devices Wednesday 24th November 2010  at 2:00pm

Overview of presentation
The three main standards for sterilization of medical devices (EN550, EN552 & EN554) were revised in 2006 and 2007 and have either came into in force in 2009 or in the case of EtO, completes the transition period in May 2010. These were major changes to the standards and all three were replaced by international versions (ISO11135, ISO11137 and ISO 17665). Requirements for compliance with these have changed – especially with respect to validation and reporting. A high level of competence is required for sterilization validation and it remains one of the most common non-conformities at notified body audits for CE marking.

 

Who should attend
These standards have implications for all regulatory, quality and engineering personnel involved with managing, validating and conducting sterilization of medical devices.

 

Benefits for attending
This webinar will give guidance to help you understand the requirements for documenting validation of sterilization as well as what a Notified Body expects to see to help you comply with the new requirements and minimise the risk of non-conformities at audits.

The Marine Equipment Directive Wednesday 8th December 2010 at 2:00pm
More Info to follow shortly More Info to follow shortly

Our webinars are free and will take no more than 60 minutes.

For more information and to reserve your place now please contact
Ashleigh Gurry,  or call on +44 (0)1489 558224.

 


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