The XClinical Blog

The WHO Global Strategy on Digital Health: What You Need to Know

In April 2019 The World Health Organization (WHO) released a draft of a digital health strategy. Known as...

Reducing the Effort of Building an eCRF

Data is the linchpin for the billions of dollars dedicated to medical studies—and the eCRF is the main...

All About Marvin: The Story of XClinical

At XClinical, we value loyalty and commitment among our staff, our customers and our partners. In fact, we...

Applications and Value of RWD and RWE

In continuation from our previous blog on what real-world data (RWD) and real-world evidence (RWE) are and

HIPAA Compliance Requirements: Keeping Clinical Trial Data Private

The Health Insurance Portability and Accountability Act (HIPAA) was introduced in 1996 in the US to...

Beyond the Clinical Trial: Real World Data and Real World Evidence

At XClinical, we are all about data, and it is our mission to make it as easy as possible to collect...

The Converging Clinical Research Environments of Drug and Medical Device Trials

Medical device development is following a similar evolution to drug development in terms of regulation....

Bringing Clinical Trial Wearable Technology Data into EDC Systems: Why It Matters

I recently spoke with Emily Mitchell, Senior Director, a member in the Biometrics Portfolio Operations...

Discover the Business Value in Selecting One Single Electronic Data Capture Solution for All Your Clinical Trials

In a recent XClinical LinkedIn post, we mentioned a discussion with a mid-pharma/biotech leader who was...

A Personal Summary of the CDISC European Interchange Conference in Amsterdam

The CDISC European Interchange Conference, May 8th and 9th, 2019 in Amsterdam focused on the advancement...