This month's pick
Why site-centric eSource beats sponsor-first EDC
Sites that own their source data run faster, cleaner studies. Here's the data.
Apr 2026 · 6 min · Strategy
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Mar 2026Regulatory
ICH E6(R3) — what it really means for DCT platforms
A practical breakdown of the latest GCP guidance and how ProCTTH maps to it.
9 min · Read
Mar 2026AI
AI form generation: from protocol PDF to live eCRF
Inside the model that turns protocol synopses into validated visit forms.
7 min · Read
Feb 2026Engagement
Patient retention is a UX problem
Five engagement patterns that lifted completion rates by 23% across our customer base.
8 min · Read
Feb 2026IoT
Wearables in regulated trials — Part 1
Choosing devices, validating data, and surviving audit.
11 min · Read
Jan 2026Monitoring
The CRA mobile app: monitoring without the laptop
How encrypted chat + remote SDV cut average monitoring visit time in half.
5 min · Read
Jan 2026DCT
Decentralized oncology — myth vs. reality
What truly works for at-home capture in solid-tumor Phase II.
10 min · Read
Dec 2025Engagement
ProCoins: paying subjects without breaking blinding
How milestone-based compensation works under FDA, EMA, and PMDA frameworks.
6 min · Read
Dec 2025Quality
Building edit checks that catch real problems
A taxonomy of edit checks and which ones actually move quality.
9 min · Read