Innovation • Feb 20, 2026
From Lab to Clinic: Making Heart Scans as Simple as Blood Tests
MCG has been proven for decades — but the technology to detect the heart's magnetic field was too expensive
and too bulky for hospitals. Until now.
In our previous posts, we introduced two ideas: first, that there is a missing cardiac test in your annual
check-up; second, that magnetocardiography (MCG) — measuring the heart's magnetic field — could fill that
gap with a 5-minute, non-contact, zero-radiation screening test.
But if MCG has such clear advantages, why isn't it already in every hospital and clinic? The answer is a
story about physics, engineering, and a technology barrier that has only recently been broken.
The old way: liquid helium and shielded rooms
MCG was first demonstrated in the 1960s. The sensors used were called SQUIDs — superconducting quantum
interference devices. SQUIDs are fantastically sensitive magnetometers, capable of detecting fields as
small as a few femtotesla (a femtotesla is one millionth of one billionth of a tesla). They remain the
most sensitive magnetic field detectors ever built.
But SQUIDs come with a crippling practical problem: they only work when cooled to near absolute zero.
Specifically, they require liquid helium at 4.2 Kelvin (−269°C). This means a SQUID-based MCG system needs
a cryogenic dewar that must be continuously refilled with liquid helium — an expensive, logistically
complex, and increasingly scarce resource.
That's not all. The heart's magnetic field (~50 picotesla) is about a billion times weaker than Earth's
ambient magnetic field (~50 microtesla). To detect such a tiny signal, SQUID systems traditionally
required a magnetically shielded room — a specially constructed enclosure lined with layers of
mu-metal and aluminium that blocks external magnetic fields. These rooms cost ₹5–15 crores to build and
occupy hundreds of square feet of hospital floor space.
New MCG (OPM-based)
Clinical-grade and scalable
- ✓ Room-temperature operation
- ✓ No magnetic shielding required
- ✓ Minimal maintenance
- ✓ Compact: fits in an examination room
- ✓ Target cost: fraction of SQUID systems
The result? Despite decades of published clinical evidence showing that MCG works — that it can detect
coronary artery disease, arrhythmia risk, and other cardiac conditions — fewer than a handful of hospitals
worldwide have ever had an MCG system. The technology was proven but impractical. The science was right;
the engineering wasn't ready.
The breakthrough: atomic magnetometers
The technology that changes everything is the optically pumped magnetometer, or OPM. Instead of a
superconducting circuit, an OPM uses a small glass cell filled with an alkali metal vapour — in our case,
rubidium-87 atoms. A laser beam is used to "pump" these atoms into a quantum spin-polarised state, and
then "probe" how that spin state evolves in the presence of a magnetic field.
The key physics is this: when rubidium atoms are spin-polarised and placed in a magnetic field, they
precess (rotate) around the field direction at a very precise frequency — the Larmor frequency — which is
directly proportional to the field strength. By measuring this precession frequency with extreme
precision, you can measure the magnetic field with extreme precision.
How it works, in one paragraph
A laser pulse polarises rubidium-87 atoms in a tiny vapour cell. The polarised atoms then freely precess
around the ambient magnetic field at the Larmor frequency (proportional to field strength). A second laser
pulse reads out this precession as a decaying oscillation — a "free induction decay" or FID signal. By
fitting the frequency of this oscillation, the magnetic field is determined. Do this hundreds of times per
second, and you get a continuous measurement of the magnetic field — sensitive enough to detect the heart.
The critical advantage: this entire process happens at room temperature. No cryogenics. No liquid helium.
No expensive dewar. The sensor is a small glass cell, a laser, and a photodetector. It can be made
compact, lightweight, and — with continued engineering — affordable.
The real innovation: no shielded room
Making the sensor room-temperature is necessary but not sufficient. The bigger challenge is operating
without a magnetically shielded room. Remember, the heart's magnetic field is about a billion times weaker
than the environment. How do you detect it without blocking out the environment?
The answer is a technique called gradiometry. Instead of using a single magnetometer, you use two — one
positioned close to the chest (measuring heart signal + environment) and one positioned a few centimetres
further away (measuring mostly environment). By subtracting the two readings, the common environmental
noise cancels out, and what remains is predominantly the cardiac signal.
This works because the heart's magnetic field falls off steeply with distance (approximately as 1/r³ for a
dipole source), while distant environmental noise is nearly the same at both sensor positions. The
subtraction preferentially preserves the nearby cardiac source and rejects the distant noise.
Using a gradiometric configuration of two scalar FID-OPM sensors, our team at GDQLabs has detected human
cardiac magnetic fields with a sensitivity of 2.6 pT/√Hz in a completely unshielded environment — no
magnetic shielding of any kind. The QRS complex of the cardiac cycle was clearly visible with a
peak-to-peak amplitude of approximately 20 picotesla.
This is the result that changes the equation. It means MCG can be performed in a normal room — a doctor's
consultation room, a diagnostic clinic, a mobile health unit. The requirement for a magnetically shielded
room, which was the single biggest barrier to clinical adoption of MCG for 50 years, has been eliminated.
A brief history of MCG — and where it's heading
1963
Baule and McFee record the first human magnetocardiogram using induction coils — a noisy,
proof-of-concept measurement.
1970s–1990s
SQUID magnetometers enable high-quality MCG recordings. Clinical studies demonstrate detection of
ischaemia, arrhythmia risk, and fetal cardiac abnormalities. Systems require liquid helium and
shielded rooms.
2000s–2010s
Two MCG systems (CardioMag Imaging, Genetesis) receive FDA clearance. Clinical evidence accumulates,
but adoption remains minimal due to cost and infrastructure requirements.
2010s–2020s
Optically pumped magnetometers (OPMs) mature as a technology. First demonstrations of OPM-based MCG.
Early systems still use lightweight shielding.
Now
Scalar FID-OPM technology enables fully unshielded MCG. Room-temperature, compact, no cryogenics, no
shielding. For the first time, the engineering matches the science.
Who would benefit?
If MCG becomes a routine clinical tool — a 5-minute, non-contact test costing less than ₹8,000 — the
potential impact is enormous. The populations who stand to benefit the most are:
1
Adults over 40 with risk factors
High blood pressure, diabetes, high cholesterol, smoking, or family history of heart disease. These
individuals have the highest pre-test probability of subclinical coronary artery disease.
2
Post–heart attack follow-up
Patients who have already had a cardiac event need regular monitoring for re-stenosis and arrhythmia
risk — currently done with stress ECG, which has limited sensitivity.
3
Pre-operative cardiac clearance
Before major surgery, patients need cardiac clearance. A rapid, non-invasive MCG test could replace
slower, more expensive alternatives.
4
Healthy adults — peace of mind
Routine cardiac screening alongside the annual blood panel, for anyone who wants to know that their
heart is healthy — the same way they check cholesterol every year.
What GDQLabs is building
At GDQLabs, we are developing a portable, magnetic-shield-free MCG system based on scalar
free-induction-decay optically pumped magnetometers. Our system uses rubidium-87 vapour cells operating at
room temperature, in the Earth's ambient magnetic field, without any magnetic shielding.
We have already demonstrated human MCG recordings in a completely unshielded laboratory at IISER Pune,
detecting QRS complexes across multiple chest positions with clear polarity reversal — confirming that the
system has genuine spatial sensitivity to the cardiac source.
The roadmap ahead involves scaling from a single gradiometric sensor pair to a multi-channel array,
developing machine-learning-powered diagnostic software, pursuing regulatory clearance, and conducting
clinical validation studies. The goal is a system that can be deployed in hospitals and clinics as a
routine cardiac screening platform — making MCG as accessible and routine as a blood test.
The vision
A 5-minute, non-contact, zero-risk cardiac screening test — as routine as a blood cholesterol panel — that
can tell you whether there is evidence of heart disease forming, before your first symptom.
For fifty years, MCG has been a technology that works but couldn't scale. The physics was proven. The
clinical evidence was strong. But the engineering demanded liquid helium, shielded rooms, and
million-dollar budgets.
That era is ending. Room-temperature quantum sensors, operating in Earth's ambient field without
shielding, are making MCG practical for the first time. The science finally has the engineering it
deserves.
The missing test in your annual check-up may not be missing for much longer.
Want to learn more about GDQLabs and our MCG technology?
We're building the future of cardiac screening. Follow our journey.