From lab to commercialization, Armstrong Clinical offers biopharmaceutical companies and medical research institutes expertise in clinical development strategy and study design. Our services help build confidence your studies and programs will reliably and effectively meet your vital clinical development targets.
Before you begin, Armstrong Clinical can advise you of your clinical, regulatory and commercial requirements at each stage of development to plan your clinical strategy and risk mitigation accordingly.
Armstrong Clinical specializes in early phase clinical development strategy. Our expertise will reduce time while improving the chance that your studies will deliver discernible outcomes.
Regional clinical practices and study dynamics must be considered when designing effective and efficient studies. We have managed study design and implementation in over 30 countries to understand how your study locations affect your risk and your commercial, cost, and time objectives.
Predictive modelling for more accurate dose selection, adaptive design, remote monitoring, PK/PD analysis using pharmacometrics. Understand when and how modern tools can be used in your develpoment programs to increase the probability of success and decrease development cost and time.
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