A successful registry requires careful planning. Discussions regarding the patient population, selection of relevant variables, definitions of variables, data collection issues, and compliance are paramount in registry development. All ethical and patient privacy requirements are addressed during this planning phase.
Quality data is critical to draw accurate conclusions about your study population. Comprehensive data collection methods are developed based on the outcome endpoints of interest and the population to be studied. Careful attention is given to the aspects of collecting, cleaning, storing, reviewing and reporting data in the registry. Training and technical support are provided. Archival and data retrieval procedures, along with documentation controls are in place so that QA requirements for compliance are met.
Because our registries are web-based, our clients have the ability to analyze their registry data at any given time. We work with our clients to determine the type of information to be extracted from the registry database and how the client would like to view the results. Standardized reports summarizing the registry data can be generated with a push of a button. Reports that profile patient enrollment, demographics, efficacy and safety are just a few of the many kinds of reports available. As a result, you can extract accurate information as your study progresses.
A ClinSmart statistician can provide statistical support throughout the registry process. The statistician can assist in registry design. He or she can also provide support in determining how to analyze, interpret and report the registry data. In addition, the statistician can work together with a medical writer to assist in developing manuscripts for publication.
Our writers can assist you with coordinating, organizing and summarizing the results of your study. We can help interpret your results and provide advice on the best way to present your results for possible manuscript publication.