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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What Defines Quality in Medical Writing?
Several pieces of research say the majority of medical writing services are sold on the basis of quality, but what really is quality and why do medical writers think it is so important? Learn more about what defines quality in medical writi...
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ICH GCP E6 Addendum R2 - What do you need to know?
Explore the ICHGCP E6 Addendum R2 changes and what they mean for sponsors and vendors in clinical trial conduct, risk-based monitoring and emerging technologies
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mHealth Apps and Wearables in Clinical Trials to Consider
A Quanticate blog exploring the use of consumer-grade mHealth apps and wearables in clinical trials and the most recent regulations on mobile health
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![Quality Process Improvements and SOP Updates [Infographic]](https://www.quanticate.com/hs-fs/hub/22135/file-13431533-png/images/quality_process_improvement1-resized-600.png?width=800&name=quality_process_improvement1-resized-600.png)
Quality Process Improvements and SOP Updates [Infographic]
A Quanticate infographic exploring Quality Process Improvement and how we ensure our SOP Updates comply with regulatory changes.
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Quality Assurance in Clinical Trials – An Introduction to GCP
Quanticate look at one part of Quality Assurance in Clinical Trials which is adhering to Good Clinical Practice (GCP)
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