Blog

Come see us at OCT Europe 2025

Visit us at booth #31 to discover a simpler way to handle data capture and management in clinical trials—let’s talk about how ShareCRF can help.

Medical Coding in Your EDC: Fewer Errors, More Time for What Matters

Tired of dealing with messy, inconsistent data? Integrated medical coding in your EDC can help reduce errors, save time, and make analysis easier. In this article, we explain how it works and why it could make a real difference in your next clinical trial—without overcomplicating things.

Targeted SDV for Risk-Based Monitoring

How did we move from checking every single data point in clinical trials to verifying only what really matters? Discover how Targeted SDV reshaped monitoring—saving resources and improving quality without losing control.

How to make mid-study changes as if you had an army of computer scientists but without having to program a single line of code.

According to a survey done by Tufts Center for the Study of Drug Development among 194 corporations involved in clinical trials, changes mid-study are the largest headache for these organizations. Every single change takes an average of 30 days to be performed and there is usually an average of 4 planned and 4 unplanned changes in a study.

IVDR and Performance Evaluation: Your Plan to Manage Data Without Hassle.

Comply with the IVDR and manage performance data for your IVD device efficiently and securely. Discover how ShareCRF simplifies compliance with its validated EDC system.

ePRO/eCOA in clinical trials: 3 keys to save a lot of time.

The acronyms ePRO and eCOA define the tools used to collect data directly from the participants in clinical trials.

Pseudonymisation in clinical trials: dissociation vs encryption

Discover the advantages and inconveniences of these two pseudonymisation methods used in clinical research

Clinical trials and GDPR

In clinical trials and studies a large number of data on the participants is required to be stored and managed. Is that clinical data subject to compliance with the GDPR?

3 Advantages of using a visual editor to create an eCRF

If you need to create an eCRF for your clinical study, let me give you a piece of advice: use an eCRF that allows you to design and configure it through a visual editor.

The 3 keys to not fail when choosing an eCRF.

If you have decided to use an EDC or an electronic CRF (eCRF) to collect data in your clinical trial, it is important to know what are some of the most important characteristics that you should keep in mind when choosing one.

Everything You Need to Know to Comply with the MDR and Manage Clinical Data Without Hassle

Learn how to comply with MDR and ISO 14155 by managing your clinical data securely and efficiently. Discover how ShareCRF simplifies compliance with its validated EDC system