Navigating the Clinical Protocol Activation Process for Industry-Written and Sponsored Clinical Trials. The flowchart and steps below outlines the best practice for processing industry-written and ...

The need for automated metadata management software has never been greater. The number of global clinical trials being run is increasing every year. And, they are becoming increasingly complex to ...

The future of clinical data management lies in the ability to adapt to these changes and needs. In order to be truly effective, a CDM system must be able to handle large amounts of data, be ...

Lakshmi Priya Darshini Pulavarthi blends scientific expertise with data management to drive clinical trial success across oncology, hematology, and cardiovascular therapeutic areas.

Aggregating data in a central clinical data management system (CDMS) is a crucial first step since advances in technology can easily facilitate data being centralized and consolidated into one ...

The breakthrough came with the introduction of Clinical Data Interoperability Services , which leveraged the Fast Healthcare Interoperability Resources standard. 7 By providing a syntactic template ...

With a commitment to process optimization, training, and audits to enhance their operations, CROs can ensure the integrity of medications throughout the trial process. [Adobe Stock ...