Proxemis Flipbook v5

Ensure the smooth running of your clinical trial, and take care of all regulatory compliance monitoring We’ll manage your trial documentation, including a trial master file (TMF) where appropriate, and deliver clinical study supports.​ Monitoring visits will be provided during recruitment and conduct, as well as the verification of source data for audit trails.​ We’ll also handle the receipt, review, reporting and follow-up of any serious adverse events (SAEs). Investigator & site management services​

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