Clinical trials are research studies in human beings that follow a pre-defined protocol and are conducted to assess the safety and effectiveness of a new medication, therapy or device. These trials can only take place once Health Authority and Ethics Committee approval is granted in the country where the trial is taking place. Clinical trials follow different standards and regulations: Helsinki Declaration, Tokyo 2004, ICH Guidelines for Good Clinical Practice (CPMP/ICH/135/95), Health and Healthcare standardization HSS, Swedish standards SS-EN ISO 14155-1:2003 and SS-EN ISO 14155-2:2003.
Our website also serves as a forum for surgeons. In order to take part of the information that from time to time may be of confidential nature requires that you are associated to the company or involved as a surgeon or scientist in ongoing studies. To apply for login membership, please contact Marie-Louise Andersson at our office in Halmstad.
Articles or informations available for surgeons, scientists or login members.
- Literature Review CREX
- Preclinical Studies
- CREX-001 (Completed trial)
- CREX-002 (Closed Trial) (abstract)
- CREX-003 Study (ongoing study)