The vitality of documentation cannot be denied at any step in the clinical trials and research work. Governing bodies have stringent rules and protocols for adhering to the documentation. Keeping the growing need in mind the module is developed and various components have been incorporated. Essential documents in Good Clinical Practices (GCP) differ in every phase of clinical trials. This course gives complete information on the vital documents which are required at every phase of clinical trial as per the good clinical practices. The purpose of the documents for each document is also elaborated. Information and content of the files like Trial master file, investigator site file and investigator file are described in detail in this module. The course is designed by the Industry experts who are working from ages in this industry and are glad to share their rich knowledge to the interested through this online course. To gain the better insight we suggest you to enrol the online course module.
|Course Details||Duration (hours)|
|1.Essential Documents||Glance||1-1.5 hrs|
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