Larix is a full service Clinical Research Organisation (CRO), offering assistance in all aspects of clinical trials, to pharmaceutical, biotechnology and medical device companies
We provide services within statistics, data management (DM), clinical research (CR), pharmacovigilance (PV) and data monitoring committees (DMCs).
We have experience in phase I-IV trials in many therapeutic areas and have provided services to most major Danish pharmaceutical and medical device companies.
We can assist you in planning and managing all phases of your clinical trials; from initiation (e.g. clinical development plans, feasibility and patient recruitment) and conduct (e.g. data handling monitoring and document management) to close-out and finalization (e.g. close-out visits, statistical analysis and reporting).
Our Mission is to deliver high quality within agreed budgets and timeline.
Our focus is our customer's goals and their specific needs.
Larix A/S takes over the projects and employees of Norma A/S
The 24th Jul 2015, Larix A/S signed a transfer agreement with Norma A/S (including its subsidiaries) in a takeover of Norma’s employees and ongoing projects. The transfer is effective as of 1st July, 2015. For further information, please see the PRESS RELEASE.