Published by
@ShahidNShah
@ShahidNShah
The successful execution of your clinical trial hinges on the people involved day to day
DZS matches the right team to your drug or device program to ensure the highest quality data review and interaction between study sites. We have a global network of regionally based clinical research assistants and clinical project managers who are experienced and highly trained and have specialized knowledge in clinical trial monitoring procedures, regulatory guidelines and a wide range of therapeutic areas.
Features:
Identifying and developing a monitoring plan to ensure patient recruitment goals are accurately defined
Supporting identification and initiation of investigator sites
Ensuring sites are demonstrating the appropriate oversight and execution of the clinical protocol
Reviewing source documentation and resolving data queries
Overseeing data collection
Ensuring regulatory compliance
Conducting interim analyses upon request
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