Fundamentally, a registry is an observational and/or outcome study that systematically tracks clinical parameters in actual practice.
For product registries, this means that the outcome is real-life “effectiveness” as opposed to “efficacy” measured in controlled clinical trials. Registries also provide a way to satisfy public and regulatory authority concerns about long-term safety of both new and older products.
Anabase has solid experience planning, implementing, and analyzing large, multi-center trials and long-term studies in a variety of therapeutic categories worldwide. In that perspective, Anabase can be your partner of choice to do the registry you need.
Practically, we can help you, step-by-step:
• establish achievable goals
• determine your primary objective(s)
• recruit, manage, and support sites
• create optimal data collection forms
• produce easy-to-follow procedures
• capture data in a way that suits each site
• set-up in no time a customized,
web-based site and data management system
• provide a sophisticated validation program
• keep you abreast of registry progress with real-time,
web-based reports and graphs
• perform statistical analysis of results
• write the findings for publication
Registry Brochure