Safety data in clinical trials should be effectively processed since this will lead the successful conduct of the clinical trial. While having many years of experience in clinical trial management, mediSMART offers effective management of clinical trial safety from case assessment through to expedited reporting of SUSARs (Suspected Unexpected Serious Adverse Events) to Ethics Committees and Regulatory Authorities as well as submission of ASRs (Annual Safety Reports) both Ethics Committees and Regulatory Authorities on an ongoing bases during the course of clinical trial.

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