For international medtech start-ups, entering a new market means learning about the local healthcare system, understanding who makes decisions, working out who pays and finding the right way to make people care. For Aspivix, a Swiss medtech and femtech company founded in 2015, storytelling has become critical to that process. As it brings its women’s health innovation into markets including Europe, the US and beyond, Ikram Guerd, Aspivix’s Chief Marketing Officer, has learned the significant impact that a strong story can have on investors, clinicians and patients.
Aspivix originally planned to enter Europe before moving into the US. How did that strategy change?
As a Swiss company, our goal was to enter Europe first. Back in 2021, we only had seven people in our team, but today we’re 14 from various backgrounds: French, Swiss, Belgian, Italian, American, Indian, Chinese and Greek. Europe seemed to be the right place to gather evidence and build a foundation before bringing the technology to the US. However, we received FDA 510(k) clearance before the CE mark approval, so we shifted our strategy to focus on the US earlier than expected.
One belief European or Swiss companies hold is assuming they can duplicate their local approach in the US, but it can’t be copy-pasted. Customer behaviour, the healthcare system and reimbursement processes are all so different. You cannot treat Europe as a test market and then move to the US thinking everything will be transferable.
Have you looked at entering other markets?
The US remains the biggest market in reproductive health, so that’s our focus, but we are looking at different markets to bring our innovation to women worldwide. In parallel, we’ve started exploring new regions like South Asia, Latin America and the Middle East. These targets were not our primary markets, but they emerged mostly through distributors reaching out to us. Bayer, who was also our early partner in Switzerland, has a subsidiary in Israel interested in bringing our product to their market.
In Brazil, we now have clearance for our product in the market, which has given us access to a successful strategy: gathering clinical evidence at a low cost in high volume. Brazil provides such a large number of IUD placements (our main clinical indications) that, within just one hospital, there can be more than 600 patients who can be enrolled very easily within around six months. This allows us to gather the data and clinical evidence the product needs to become available more widely. That’s something you cannot do easily in the US or in Europe in terms of budget or speed.
