Write a Crown SOP and related forms on Handling Adverse Events

Write a Crown SOP on Data Retention for PV and CR

Write a Crown SOP on Good Documentation Practice

Write a Crown SOP on Literature Review for marketed products

Write a Crown SOP for reporting of adverse events by investigators to the sponsor

Write a Crown SOP and Archiving Procedure and Forms for PV and CR documents

Write a Crown SOP on Investigators' responsibilities for reporting all categories of SADRs

Write an SOP for creating and maintaining the Detailed Description of Pharmacovigilance System for a company

Write a Crown SOP on creating a DSUR for Clinical Trials