I see a lot of US-centric discussion about compounded semaglutide on this forum, so I wanted to start a thread for Europeans to understand our very different regulatory landscape.
The fundamental difference: In the EU, compounding is governed by Directive 2001/83/EC, Article 3, which allows pharmacy compounding only for individual patients with a prescription, and only when no authorised equivalent exists on the market.
Since Ozempic and Wegovy are authorised in the EU via the EMA centralised procedure, compounding semaglutide is essentially illegal in most EU member states.
This means the US model — where compounding pharmacies make semaglutide because of "shortage" designations — simply doesn't apply here. There's no shortage exemption in EU pharmaceutical law in the same way.
So what are Europeans actually doing? Let's discuss country by country.