White Paper: Unintentional Unblinding

 
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Maintaining the study blind is a critical part of maintaining the integrity and validity of any clinical trial. Experienced IRT providers have a variety of SOPs, system controls and well-trained members of staff to ensure that all blinded reports, data transfers and study documentation and communications are sanitized and free of any sorting or data that could even partially reveal the study medications in inventory or those assigned to patients.

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