There are no regulations in the USA or EU that specifically govern case report form development or data management practices. There are some guidelines produced by professional bodies of data managers. This presentation will cover the range of data management tasks from CRF design to data entry to raising and resolving queries to tracking all aspects of data management.
There will be a short discussion of importation of data as well as safety management as it pertains to data management. Throughout the presentation, general guidance on best practice will be given.
This audio conference is presented Helen Colquhoun, MD, CEO of Pleiad Devices. For more information of Data Management for Medical Device Trials: Best Practices, please visit our site www.fxconferences.com
