Imagine presenting PMCF data to your Notified Body and being asked:
“How can you prove this dataset hasn’t been altered?”
For most survey systems, the honest answer is:
“We can’t, not completely.”
That’s a problem.
Because MDR has shifted expectations from:
“plausible data”
to
“provably trustworthy data.”
The weakness of traditional tools
Legacy systems rely on:
- manual logs
- spreadsheets
- editable records
- post-hoc reconciliation
Which creates:
- integrity doubts
- audit burden
- manual verification loops
- compliance risk
Even well-run studies struggle to prove immutability.
A different approach: integrity by design
1SURVEY+ embeds compliance directly into the data capture process
Every action is:
- timestamped
- certified
- notarized
- immutable
using blockchain technology.
This means:
- no retroactive edits
- full traceability
- automatic audit trails
- instant verification
Evidence is trustworthy from the moment it is created.
Not validated afterward.
Why this is unique
Most platforms store data.
1SURVEY+ certifies data.
That’s a fundamental difference.
It allows manufacturers to:
- eliminate manual QC loops
- accelerate reporting
- simplify audits
- defend evidence with confidence
And opens the door to advanced engagement features like secure incentives and verified participation.
Supported by clinical expertise
Importantly, this isn’t just technology.
It’s delivered with:
- regulatory strategy
- clinical methodology
- biostatistics
- medical writing
- PMCF reporting
So the data isn’t only secure — it’s scientifically defensible.
Bottom line
In a world where regulators demand proof of integrity, ordinary survey tools aren’t enough.
Certified, immutable evidence is becoming the new standard.
And that’s exactly what 1SURVEY+ was built to deliver.
Schedule a demo to see how 1Survey+ turns feedback into product intelligence demo@1med.net
