Stiris’ safety team provides a comprehensive range of Medical Affairs and Pharmacovigilance services throughout the product life cycle. The Medical Monitor is an integral partner throughout the trial, collaborating across functional units to assist you in effectively managing your drug safety information.
Medical Affairs and Pharmacovigilance Services include:
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Highly qualified and experienced Physicians who know industry standards, methodology and regulations.
Ensuring the accuracy and integrity of clinical trial data while always ensuring patient safety.