Tool

Your CMRR is not the datasheet figure.

The electrodes and the input impedance form a divider, and any mismatch between them turns common-mode interference into a differential signal before the amplifier has a say. This works out which of the two is actually limiting you.

The interference path

Two things reject common-mode interference and only one of them is on a datasheet. The electrodes and the amplifier's input impedance form a divider, and any mismatch between the two electrodes converts part of the interference into a differential signal the amplifier cannot tell from your biosignal.

V
Mains coupling on the body. Volts, not millivolts, in a typical clinical room.
dB
The datasheet figure, at the frequency you care about rather than at DC.
kohm
The difference between the two electrodes, not their absolute value. Grows through a recording as gel dries.
Mohm
uV
uV
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Where the rejection actually comes from
TermResidual at the inputEquivalent rejectionShare
Amplifier rejection15.8 uV110 dB39%
Electrode imbalance25.0 uV106 dB61%
Total at the input40.8 uV102 dB effective100%
Effective CMRR
102 dB
Datasheet says 110
Given away to imbalance
8 dB
Signal to interference
1.8 dB
Interference vs noise floor
40.8x
Interference dominates the floor
Your effective CMRR is 102 dB, not the 110 dB on the datasheet. The electrode imbalance is throwing away 8 dB before the amplifier has any say in it. At this signal-to-interference ratio the recording is not usable without further filtering, and filtering at the mains frequency takes physiology with it.
Send me this budget

Your numbers go with it. If the imbalance term dominates, the fix is in the electrode and the input stage rather than in a better instrumentation amplifier, and that changes the bill of materials conversation.

Your inputs are included so the reply can be specific.

Rejection from the electrode divider alone

What the electrode path gives you before the amplifier contributes anything, by impedance mismatch and input impedance. Compare a row against the CMRR on your amplifier's datasheet: wherever this figure is lower, the electrodes are the limit and a better amplifier buys nothing.

Mismatch100 Mohm input500 Mohm input1 Gohm input10 Gohm input
0.5 kohm106 dB120 dB126 dB146 dB
1 kohm100 dB114 dB120 dB140 dB
2 kohm94 dB108 dB114 dB134 dB
5 kohm86 dB100 dB106 dB126 dB
10 kohm80 dB94 dB100 dB120 dB
20 kohm74 dB88 dB94 dB114 dB
50 kohm66 dB80 dB86 dB106 dB

Red is below 90 dB, amber below 110, which is roughly where a good instrumentation amplifier sits. A cell in red means the amplifier specification is irrelevant: the electrodes have already decided the outcome.

A worked example

A wearable EEG front end specified with a 110 dB instrumentation amplifier and a 1 gigohm input impedance, recording 50 microvolt signals in a room with about 5 volts of mains coupling on the body. The bench results are clean and the part selection is not in question.

The amplifier contributes 15.8 microvolts of residual. A 5 kilohm electrode mismatch, which is unremarkable for dry contact partway through a session, contributes 25 microvolts on its own. The two together give an effective CMRR of 102 dB, so eight decibels have gone before anyone wrote firmware, and the electrode path is already the larger term.

The number that matters clinically is the last one: 41 microvolts of interference against a 50 microvolt signal is 1.8 dB of signal to interference. The physiology is not swamped, but it is not comfortably above the noise either, and the mismatch is the term that grows as the session runs.

Which makes the design decision a materials and contact one rather than a semiconductor one. Improving the amplifier to 120 dB moves the total from 41 to 30 microvolts. Halving the mismatch moves it to 28. Doing both is not twice as good as either, because the two terms add and the smaller one stops mattering.

The arithmetic, so you can check it

The amplifier contributes Vcm / 10^(CMRR / 20). The electrode path contributes Vcm x mismatch / input impedance, because the divider formed by the two electrodes against the input impedance is unbalanced by exactly that ratio. The two residuals add at the input, and the effective rejection is 20 x log10(Vcm / total residual).

The honest limit

This is the resistive case at a single frequency, which is the right first calculation and not the whole story. Real electrodes are complex impedances that vary with frequency, so the mismatch at 50 hertz is not the mismatch at 500, and cable capacitance adds a path this does not model. Treat the result as the floor on your interference rather than the total, and measure the real thing on the real electrodes before you commit the bill of materials.

The physical reasoning is in common-mode rejection explained, and the constraint a driven reference introduces in the driven reference electrode. If you are adding one, check its margin with the return-path calculator before the board exists.

Questions

Why is my effective CMRR worse than the amplifier's datasheet figure?

Because the electrodes and the amplifier's input impedance form a divider, and any mismatch between the two electrodes converts part of the common-mode interference into a differential signal before the amplifier sees it. That path has its own rejection figure, set by the ratio of input impedance to mismatch, and the two combine. A very good amplifier behind a poor electrode balance behaves like a much worse amplifier.

What impedance mismatch is acceptable for a biosignal front end?

It depends on your input impedance, which is why the ratio matters rather than the absolute figure. A 5 kilohm mismatch against a 1 gigohm input gives about 106 dB of rejection from that path alone, which is already comparable to a good instrumentation amplifier. Against a 100 megohm input the same mismatch gives 86 dB, and the electrodes are then unambiguously the limit.

Should I design for the mismatch at setup or during the recording?

During, and at the end. Electrode impedance mismatch grows through a session as gel dries and contact degrades, so the figure at setup is the best case and the one at the end of the longest expected recording is the one to design against. A front end that meets its specification only in the first ten minutes will pass a bench test and fail in clinic.

Does a driven reference electrode fix this?

It reduces the common-mode voltage on the body, which lowers the interferer term rather than improving the rejection ratio, and that helps both paths at once. It also introduces its own constraint: the current it drives has to return through the electrode, and the amplifier doing the driving has to be able to sink it without railing. That is a separate calculation and it is worth doing before the board exists.

Can I filter the interference out instead?

Only partly, and it costs you signal. A notch at the mains frequency removes physiology sitting at that frequency along with the interference, and the harmonics remain. Filtering is a reasonable last layer over a front end with adequate rejection; it is not a substitute for one, because it cannot recover a signal that has already been swamped at the input.