Understanding CDISC Standards in Clinical Research: A Practical Guide
Clinical research generates a large amount of data: protocol-defined assessments, CRF data, laboratory results, adverse...
SWISS BIOTECH DAY 2026 is coming up, and TUNECT will be there
This year, our team brings three perspectives to the same table: #Strategy - how Sponsors...
World Health Day – April 7| A small reminder from our team
In our field, “health” is usually discussed through protocols, evidence, safety, and outcomes. And rightly...
What 2026 conference agendas are really signaling and what it means for sponsors and CROs in clinical trials and biometrics
This is not a “we were at a conference” post. It is a market read...
Big product update from TUNECT: introducing the Automatic Protocol Amendment Harmonizer™
From today, every protocol amendment will instantly and perfectly align: - the SAP - CRF...
What is a Functional Service Provider (FSP) in Clinical Research?
How does a CRO interact with a sponsor? What is project-based delivery, what is FSP...
GCP in Practice: Principles 10-11 of ICH E6(R3)
We’re closing our E6(R3) series with two principles that most often decide whether execution stays...
GCP in Practice: Principles 7-9 of ICH E6(R3)
Now we move from design principles to making execution feasible and ensuring the results are...
GCP in Practice: Principles 4-6 of ICH E6(R3)
In the last post we covered Principles 1-3 (ethics, consent, independent review). Now we move...
GCP in Practice: Principles 1–3 of ICH E6(R3)
We’re starting the series on the 11 principles of ICH E6(R3). E6(R3) consolidates and reframes...