Document titled GPSR with a magnifying glass placed over a warning sign
General Product Safety Regulation (EU) 2023/988 obliges
GPSR Risk Analysis Required

Mandatory for almost every product: According to the GPSR, producers must draw up technical documentation for the products they place on the market. The technical documentation must be based on an internal risk analysis.

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General Product Safety Regulation requires Responsible Person
EU Responsible Person Service for the GPSR and more

Since 16 July 2021, it is against the law to sell products with CE marking without a Responsible Person in the EU. In addition, a Responsible Person must also be specified in accordance with the General Product Safety Regulation (EU) 2023/988.

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Personal EU Batteries Regulation Training
Ready for the new Batteries Regulation (EU) 2023/1542

Find out which obligations the EU Batteries Regulation places on you and how to deal with them in your specific case. Receive comprehensive information on how to implement your obligations with regard to labelling, battery passport, EPR and due diligence obligations in the supply chain.

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Personal EU Batteries Regulation Training
Ready for the new Batteries Regulation (EU) 2023/1542

Find out which obligations the EU Batteries Regulation places on you and how to deal with them in your specific case. Receive comprehensive information on how to implement your obligations with regard to labelling, battery passport, EPR and due diligence obligations in the supply chain.

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trade-e-bility News and Press Releases

Coordinated product safety measures imposed by EU authorities are on the rise

As reported by the news magazine Umweltruf/Europaticker, the number of follow-up measures of hazard notifications to the EU Rapid Alert System such as recalls or destruction of products increased by 10 per cent year-on-year, to reach 4,477 cases. In addition, the Commission is stepping up its work on product testing with the EU member states. The Commission will further modernise the Rapid Alert System to encourage consumers to consult the alert database and make safe buying decisions. Trade-e-bility GmbH is available to answer your questions - please call +49/40/75068730-0 or send an e-mail message to beratung@trade-e-bility.de.
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WEEE in Belgium: New device list

Our Belgian WEEE take-back system has published an updated list of electrical and electronic devices that will be valid as of July 2020. The main change is the extension of the product list, which now includes some additional equipment that was not previously covered by Belgian WEEE legislation. Please check whether your products are affected.
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TMK seminars and webinars in 2020 – sign up now!

Since the corona-related interruption, take-e-way and trade-e-bility GmbH have developed a new comprehensive seminar programme for you in 2020, which we will gradually expand in the coming months.
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E-cigarettes: Marketing liquids in full legal compliance!

Distributors of e-cigarettes must always ensure that all ingredients they contain are known and declared. Germany’s state investigation offices carry out random checks in this regard. Recommendation: Not only does e-cigarette hardware need to be marketed in full legal compliance; special attention must also be paid to the liquids used.
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Corona short test for PPE masks has been revised

A simplified test procedure for the approval of PPE masks as medical masks has already been in place since the corona pandemic began. The Central Office of the Federal States for Safety Technology (ZLS) has now published a new revision of the test procedure with the issue date 2 June 2020. The new features include additional criteria for labelling the masks. Trade-e-bility GmbH will support you in selecting a suitable market access procedure and evaluating the necessary documentation.
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BfArM special approval of masks was restricted

Up until now, it has been possible to market dust protective breathing masks with test certificates for FFP2, KN95 or N95 as medical devices for customers in the healthcare sector by special approval from the Federal Institute for Drugs and Medical Devices (BfArM). According to the BfArM, many masks were unfortunately put into circulation via this route with the aid of forged certificates that fail to meet what they promise. In addition, the market is once again sufficiently supplied with regularly certified masks, which means that special approval will only be granted for masks for which a test certificate in conformity the corona test procedures of the Central Office of the Federal States for Safety Technology (ZLS) is in hand. Accordingly, for the time being KN95 or N95 respiratory masks are no longer marketable as medical devices without verification. Trade-e-bility GmbH supports you by reviewing the available documents, estimating the costs and selecting possible market access.
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Batteries Act: Are your batteries required to be registered with the EAR foundation on 1 January 2021?

The previous obligation to notify the German Federal Environment Agency (UBA) will be replaced by mandatory registration for manufacturers of device, automotive and industrial batteries. The task of registering manufacturers will be performed by the EAR foundation (German WEEE registration board) on being commissioned to do so by the UBA. From take-e-way’s perspective, it is therefore conceivable that the enforcement of the Batteries Act from 2021 will be regulated as efficiently as under the German Electrical and Electronic Equipment Act. Distributors, importers and manufacturers who have not yet registered their batteries and accumulators should take action now, without any further delay.
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Compliance support for new players on the protective clothing market

For new players in the protective clothing market, but also for those who plan to market new products, professional preparation to meet the legal requirements in force is important. Trade-e-bility GmbH supports you with research on the legal requirements as well as with the normative implementation.
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WEEE Germany: Deadline for submission of the annual statistics notification again postponed by one month

Notifications submitted after 30 April 2020 – which are actually late – will therefore not be forwarded (in coordination with) the Federal Environment Agency as the authority responsible for the prosecution of administrative offences.
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Children’s masks must be safe

Children also want to be protected in corona times. Poorly fitting FFP2 or medical masks often provide worse protection than specially adapted fabric masks (referred to as community masks). It is important in this regard, however, to observe the specific safety requirements for children. In addition to the increased requirements for the absence of harmful substances in the materials, the mask in question must also be mechanically safe. Easily detachable small parts as well as incorrect lengths of the fastening cords can be life-threatening! Recommendation: The relevant safety standards should be observed in the manufacture of children’s masks.
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