Larix is a full service Clinical Research Organisation (CRO) offering assistance in all aspects of clinical trials to pharmaceutical, biotechnology and medical device companies
Larix provides services within statistics, data management (DM), clinical research (CR), pharmacovigilance (PV) and data monitoring committees (DMCs).
With our extensive experience, we assist you in planning and managing your clinical trial in all the phases 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).
We have experience in phase I-IV trials in many therapeutic areas.
Larix has provided services to most major Danish pharmaceutical companies and to a range of biotech companies in the region.
Daily cooperation between all in-house departments involved in Larix ensures constant focus on all our diverse services.
Our Mission is to deliver high quality within agreed budget and timelines
Our focus is our customer's goals and their specific needs.
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