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On June 14th, 2023, ECHA added two new substances to the SVHC Candidate List, it contains now 235 substances.
A time-saving and stress-reducing functionality!
The business of ProductIP is developing, resulting in the hiring new staff for the team in Hong Kong.
kun je strafrechtelijk worden vervolgd als je een risicobeoordeling niet goed uitvoert?
A Twitter conversation
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.
For some, a number is easier to interpret than a date, so on the technical files page, a column 'Days to deadline' was added to display the number of days until the deadline of your technical file.