ÅKRN is a European Medical Device and In-Vitro Diagnostics CRO that can help your company get clinical trial approval / EU market approval
To accelerate innovation and approval of new treatments to aid in the battle with this global pandemic, we put our CRO team at AKRN at service in the fight against COVID-19. We can support you to perform COVID-19 related submissions to the European Competent Authorities and Ethics Committees.
To ensure we support small and mid-sized companies get their products on the market as soon as possible, we have decided to perform our services Free of Charge*.
COVID-19 Submission Services include:
- Clinical Investigation Protocol (CIP) Review
- Informed Consent Form (ICF) Review
- Clinical Trial Application Support
- Essential Clinical Site Start Up Activities
We are a team of highly qualified clinical research professionals with specific experience in medical devices and in-vitro diagnostic products. We can support your COVID19 clinical study application to the EU CA regulatory agencies and Ethics Committees.
For more information download the service information or write us at email@example.com.
*Proposal valid until 30 June 2020. Please contact us for more details on the specific services provided.