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Adaptive Clinical Trials: Revolutionizing Medical Research
5 min read

Adaptive Clinical Trials: Revolutionizing Medical Research

Clinical trials are at the very foundation of medical research and supply vital proof that new treatments are both safe and effective.  While robust, the...

When to Use Risk-Based Monitoring Tools in Clinical Trials
5 min read

When to Use Risk-Based Monitoring Tools in Clinical Trials

Risk-based monitoring guarantees the quality of clinical trials by identifying, analyzing, monitoring, and reducing any risks to the study’s quality or safety. The US Food...

What is Clinical Trial Supply Management?
5 min read

What is Clinical Trial Supply Management?

Pharmaceutical businesses consider clinical trial technology solutions to save costs, streamline study management, and preserve current study information as clinical trials become more complicated. So...

What is a Certified Copy in Clinical Trials?
5 min read

What is a Certified Copy in Clinical Trials?

More inquiries than any other issue are to trial master files (TMFs), specifically about original documents and copies. There’s a lot of misunderstanding about two...

What is Risk-Based Monitoring Technology in Clinical Trials
5 min read

What is Risk-Based Monitoring Technology in Clinical Trials

Using information from earlier studies, risk-based monitoring (RBM) is a clinical trial strategy that estimates the likelihood that a patient may have certain adverse effects....

What is ePRO in Clinical Trials?
4 min read

What is ePRO in Clinical Trials?

In a clinical study, electronic patient-reported outcomes (ePRO) enable participants to use a tablet or smartphone to report on their health and respond to questionnaires....

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