ISO/IEC 27001:2022 in Clinical Trials: Turning Data Security into a Quality Standard

ISO/IEC 27001:2022 in Clinical Trials: Turning Data Security into a Quality Standard

  • Edyta Jach
  • January 26, 2026

Data security in clinical trials underpins patient protection, data integrity, and regulatory compliance. ISO/IEC 27001:2022 provides a structured, auditable framework that supports these requirements.

Read More
ALCOA++ in Practice - A New Dimension of Data Quality

ALCOA++ in Practice - A New Dimension of Data Quality

  • Edyta Jach
  • November 7, 2025

ALCOA++ principles are no longer just a good practice — they are a regulatory expectation. Learn how to translate them into system and process requirements for data collection and management in clinical trials.

Read More
Trustworthy technologies - how to ensure the credibility of clinical trials in the digital era?

Trustworthy technologies - how to ensure the credibility of clinical trials in the digital era?

  • Edyta Jach
  • October 27, 2025

Digitalization of clinical trials offers enormous opportunities, but also demands a new approach to quality and data management.

Read More
Welcome to GoResearch™.live!

Welcome to GoResearch™.live!

  • 2KMM
  • May 27, 2025

We’re launching GoResearch™.live, our next-generation eCRF platform — designed to meet the needs of modern clinical trials!.

Read More