Want To Know More About Us?
At ACliRA Consulting ApS, we follow certain collaboration principles that ensure the best possible outcome for you as our client and your project. We understand the importance of your project for your company and strive to give best possible support.

What makes the difference:
Special Knowledge adds value!
We have gathered a wealth of expert knowledge that will help you avoid mistakes and pitfalls that other players in the field usually stumble upon.
Profound experience
More than 20 years of experience in clinical development across various indications
Aerosol expert knowledge
Profound expert knowledge in aerosol medicine for the successful development of both inhaled medicines and medical application devices
Sleep Medicine expert
Longstanding experience in sleep medicine diagnostics and treatments, evaluation of sleep study results
FAQ
Frequently Asked Questions
Do you have a track record of projects / devices / compounds you have worked on?
While we generally have confidentiality agreements in place with all our clients, it is possible to obtain an overview of the device types and pharmaceutical classes of compounds we have worked on if requested. Please send us a note with the respective request, and we will be in touch!
Can you guarantee success of our clinical trial or development project?
The clinical development of pharmaceuticals and/or medical devices is a complex process, incorporating numerous factors that influence success or failure. You can leverage our vast experience to increase the chances of a successful development, and rest assured, we are dedicating our passion for clinical development to your product. But of course, we cannot guarantee that your trial or project will be a success.
My company is not based in the EU (yet). Can we nevertheless perform clinical studies in Europe?
According to Article 74 of the clinical trial regulation (CTR) of the European Union, a study sponsor must be established in a country of the European Union. If this is not the case, the sponsor can appoint a legal representative based in the EU, who acts as the official liaison between the sponsor and EU regulatory bodies (Competent Authorities) and Ethics Committees. ACliRA Consulting Aps can provide this role for your company without limitations. Please contact us for further details.
Our clients and partners
Latest News
Important Phase 1 study for Zapnometinib published
In close collaboration with fellow scientists, ACliRA Consulting ApS participated in the publication of an important…

Today is World Sleep Day…
Today is World Sleep Day…. Healthy sleep has been and still is the foundation of a…
Novo Nordisk Foundation funds BII
Big step for funding opportunities in Denmark and Europe: The Novo Nordisk Foundation granted a research…







