Larix is a full-service clinical contract research organisation (CRO) offering assistance in all aspects of clinical trials, including monitoring, trial management, data management, statistics, medical writing, pharmacovigilance and DMC. Our customers are pharmaceutical, biotechnology and medical device companies. Larix provide you with flexible solutions tailored to your needs as we do not have a rigid company policy e.g. you can outsource a specific task or the full service from development plans to final reporting and you can in-source a consultant part time or full time. We have our own standard operating procedures (SOPs), or we can work according to Sponsors SOPs. Larix has provided services to a range of companies from the smallest biotech to the major pharmaceutical companies. Our highly motivated and professional staff has experience in clinical development within both medicinal products and medical devices. Daily cooperation between all Larix in-house departments ensures pro-activity and quality on time as our focus is our customers’ goals and their specific needs. Our mission is to deliver high quality within agreed budget and timelines. .