Managing Data Challenges in Clinical Studies with a Data Safety Monitoring Board
Explore the essential functions of a Data Safety Monitoring Board (DSMB) and the crucial role data management plays in supporting its activities.
Explore the essential functions of a Data Safety Monitoring Board (DSMB) and the crucial role data management plays in supporting its activities.
Regulatory Writing is used to create a variety of clinical documents. Such clinical trial documentation includes clinical study reports. Learn more
As industry regulators and study participants seek disclosure of information in clinical trials, medical writers are creating Plain Language Summaries
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...
17 Easy steps for compiling the appendices of a clinical study report to help clinical regulatory writers in the pharmaceutical industry.
A blog looking at the number of unique challenges that a medical writer might encounter while writing / managing patient / safety narrative projects.
Quanticate looks at SAS and WinNonlin as PK analysis tools. The pros and cons of either model in deciding how to handle your Pharmacokinetic data.
A Quanticate blog article on managing multiple priorities in regulatory writing and medical writing tips to help manage projects efficiently.
What to consider and research when choosing a career as a regulatory writer in the clinical world by Quanticate.