Literature Intake

The Drug Safety team receives literature data from JAPIC and from 海外医薬情報研究会 (World Medical & Drug Information Service - WMDIS). This data includes a literature list of the company related drugs.

The Safety team assesses the content and then decides reportability for each literature information on the list, such as Research Reports, Adverse Event (AE) reports and Not-Related.

You can import these literature data files and then assess the reportability. You can book-in all neccessary data as an Adverse Event report case or as a Research report case.

For more information, see:

• Import literature files
  
• Import tab field descriptions
  
• Import tab actions
  
• Processing tab field descriptions
  
• Processed tab field descriptions