News Legal Alert life sciences
Thursday July 2nd, 2020
Sorry, this entry is only available in Polish.
Sorry, this entry is only available in Polish.
SK&S’ transaction team has advised AniCura AB in the acquisition process of veterinary clinic “Centrum Zdrowia Małych Zwierząt” in Poznań,…
According to the EU Directive, Member States shall ensure that medicinal products which are Over-The-Counter Drug (OTC) are offered for…
At the end of June, the European Commission (EC) published an updated “Blue Guide”, which, first published in 2000, has…
“SK&S’ transaction team has advised AniCura AB in the acquisition process of veterinary clinic “Gliwcka Przychodnia Weterynaryjna”. One of the…
We are pleased to inform that veterinary clinic “Animal” located in Łódź has joined AniCura, a family of leading veterinary…
On March 21, 2023, the long-awaited act on clinical trials of medicinal products for human use was signed by the…
Nicotine pouches (which we wrote about in the report) are not covered by any specific regulations in Poland. In particular,…
Electronic cigarettes, especially disposable ones, have recently been the subject of public debate, primarily due to the announcement of restrictions…
During a January meeting of the Parliamentary Committee on Economy and Development,[1] the President of the Office of Competition and…
EU regulations on medical devices (MDR[1]) and in vitro diagnostic medical devices (IVDR[2]) have been applied for several years now…
DISTRIBUTION Possible ’faster’ export/sale of products included on the list of products facing potential shortages in Poland. The Main Pharmaceutical Inspectorate (GIF) will be able…
As we informed in a last SK&S report, electronic cigarettes, particularly disposable ones, have been the subject of public debate…
RESTRICTIONS ON TRADE Adding more products to the anti-export list (the requirement to report export to the Chief Pharmaceutical Inspectorate (GIF) 30 days…
We are proud to announce that in this year’s edition of The Legal 500 we have been recommended in 13…
The introduction of Regulation (EU) 2017/745 on Medical Devices (“MDR”) gave rise to a number of questions regarding products which…