CRF Design for Oncology Trials
Explore key considerations in Case Report Form (CRF) design for oncology clinical trials, highlighting the unique challenges in this therapeutic area.
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5 Key Steps of eCRF Design in Clinical Trials
Make sure you follow these 5 steps of eCRF design to ensure the appropriate data is collected and can be used for the analysis of your clinical study.
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4 ways to Improve Clinical Data Quality in the Digital Era
Clinical Data Quality is of the utmost importance when working towards a regulatory submission. These 4 methods are a must have in the new digital era.
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Remote Monitoring During Clinical Trials - COVID-19 Update
Remote monitoring in clinical trials has never been so popular. This article explains a risk-based approach to remote monitoring and remote SDV
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First Steps in Laboratory Dataset in SAS
The laboratory dataset is one of the core safety datasets and, at first glance, it could appear intimidating. This article will illustrate checks that are worth applying at the very beginning of programming work – these could be in addition...
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Implementing Electronic Data Capture (EDC) systems in Clinical Trials
This Quanticate blog examines the implement of electronic data capture (EDC) systems in clinical trials by highlighting the benefits of moving away from paper-based studies, the thought behind the EDC database design and role of outsourcing
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Electronic Data Capture Systems In Clinical Data Management: The myths and the reality
This blog explores myths of electronic data capture (EDC) systems in clinical data management and how it is not always expensive or time-consuming to set up
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The Challenges of Writing Patient / Safety Narratives
A blog looking at the number of unique challenges that a medical writer might encounter while writing / managing patient / safety narrative projects.
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