Statplus Service > Clinical Trial > Clinical Report Writing
Clinical Report Writing
Clinical Report Writing
1. Before the final report is submitted to the client, StatPlus will review the draft report internally to ensure accuracy and completeness. The draft report will be revised to incorporate the client's comments, and the revised report will be considered final and submitted to the client for approval.
2. Upon completion of the project, StatPlus will provide the client with both raw and derived SAS datasets in transport format along with comprehensive documentation. This documentation will include information on the data cleaning and processing steps that were undertaken.