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On 21 May, the European Commission released a proposal to postpone the battery due diligence obligations by 2 years. Today the Council adopted the law.
The European Parliament does not approve the current methodology for the risk categorisation of countries under Deforestation Regulation (EU) 2023/1115
Yesterday, the European Commission shared the official risk classification list for the EU Deforestation Regulation.
Some scientists estimate that the average person eats 5 grams of microplastics per week - about the weight of a credit card. Massive amounts of microplastics pollute our surface waters.
On the threshold of a new year we changed the approach for the Verifeyer smart forms for specific hazards.
The obligation in Article 16 of Outdoor Noise Directive 2000/14/EC to send a copy of the EU Declaration of Conformity has been revoked.
Products are often discarded although they can be repaired. This results in 35 million tons of waste, 30 million tons of resources and 261 million tons of greenhouse gas emissions in the EU per year.
The new version of the ProductIP app brings regulatory knowledge at your fingertips
Stay Ahead of the Game: The current EU Toy Safety Directive 2009/48/EC will be replaced with new Toy Regulation soon. Learn About the Latest EU Toy Regulation Updates!
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kun je strafrechtelijk worden vervolgd als je een risicobeoordeling niet goed uitvoert?
In the workflow dialog, we added a new field 'Workflow deadline' to indicate when you expect the current workflow status to be resolved.
We added a region filter on the technical files page and in the file list report.
To improve traceability, whenever someone changes the risk classification of a technical file, it is now logged to timeline.
The regulatory database is now freely available for authorities. On 22 and 23 September, the so-called Deutsche Marktüberwachungskonferenz was held from Berlin in an online setting.
Increasingly complex regulatory requirements in Europe result in more companies in Hong Kong needing support.
We added a new column 'Workflow history' to the file list report. It shows a chronological list of workflow status changes for each file in the report and includes change date and status.
For medical devices it is mandatory to have Basic UDI-DI / Global Model Number.