The XClinical Blog

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...

A Brief Look at Electronic Data Capture (EDC) in Clinical Trials: Past, Present, and Future

What is EDC? Electronic data capture (EDC) is a way to record medical data digitally instead of in the...

The MedDRA and WHODrug Dictionaries: What Are They and How Are They Used?

Using medical dictionaries to code clinical trial data is a key way to ensure that your clinical trial...

How Electronic Data Capture Supports Patient Reported Outcomes in Clinical Trials

In recent years, we have seen a move towards putting patients at the heart of healthcare and clinical...