Regulatory Writing – An Integral Part of Clinical Research
Regulatory Writing is used to create a variety of clinical documents. Such clinical trial documentation includes clinical study reports. Learn more
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Get ready for Plain Language Summaries in Medical Writing
As industry regulators and study participants seek disclosure of information in clinical trials, medical writers are creating Plain Language Summaries
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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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Exploring CDISC Analysis Data Model (ADaM) Datasets
A Quanticate blog post exploring Analysis Data Model and ADaM Datasets, and how it is widely used in the submission of clinical trial information.
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Compiling the Appendices for a Clinical Study Report
17 Easy steps for compiling the appendices of a clinical study report to help clinical regulatory writers in the pharmaceutical industry.
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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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!['Clinical Trial Transparency and ALLTrials' by Ben Goldacre [Video]](https://www.quanticate.com/hs-fs/hub/22135/file-2523594494-jpg/Ben_Goldacre_Clinical_Data_Transparency.jpg?width=800&name=Ben_Goldacre_Clinical_Data_Transparency.jpg)
'Clinical Trial Transparency and ALLTrials' by Ben Goldacre [Video]
Watch Ben Goldacre discuss Clinical Trial Transparency and 'AllTrials: Transparency is moving forwards, the pharmaceutical industry can benefit from doing the right thing'
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Medical Writing Tips For Managing Multiple Priorities
A Quanticate blog article on managing multiple priorities in regulatory writing and medical writing tips to help manage projects efficiently.
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Becoming a Regulatory Writer
What to consider and research when choosing a career as a regulatory writer in the clinical world by Quanticate.
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