You can develop a new drug and bring it to market faster and more efficiently with our clinical solutions. Supporting all phases of clinical development, from early-phase exploratory studies to late-phase pivotal trials, we offer a wide range of services, including protocol development, clinical trial management, medical monitoring, data management, biostatistics and regulatory support. Navigate the complex landscape of clinical development with our team of experienced clinical researchers. We work closely with you to design and implement studies designed to meet your specific needs and goals.
With your investigational new drug (IND) or investigational medicinal product dossier (IMPD) authorisation in hand, the first-in-human or phase 1 study is the launching point of your clinical development.
To ensure a smoothly conducted study, our bioanalysis, immunology and safety laboratories are conveniently gathered under one roof together with our clinic unit. For dose escalation studies, we enroll healthy volunteers, special populations and patients, and we also have strong experience in respiratory clinical studies.
For each study, data management, statistics and monitoring are managed by experienced statisticians and statistical programmers working seamlessly with our data management team. With our successful experience in multiple therapeutic areas, you can entrust our corporate project management experts with your most challenging requests, while our regulatory affairs team can support you with scientific writing of IMPDs and a clinical development plan (CDP) tailored to your product.
Our clinical solutions include:
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