We present the first ever broadband, calibrated electrical connection to the inside of a cell. The interior of a vital, living cell contains multiple dynamic and electrically active organelles such as mitochondria, chloroplasts, lysosomes, and the endoplasmic reticulum. However, little is known about the detailed electrical activity inside the cell. Here we show an ultra-high bandwidth nano-electronic interface to the interior of living cells with integrated fluorescence readout of metabolic activity. On-chip/ on-petri dish nanoscale capacitance calibration standards are used to quantify the electronic coupling from bench to cell from DC to 26 GHz (with cell images at 22 GHz). The interaction of static to high frequency electromagnetic fields with the cell constituents induce currents of free charges and local reorganization of linked charges. As such, this enables a direct, calibrated, quantitative, nanoscale electronic interface to the interior of living cells. the interface could have a variety of applications in interfacing life sciences to nano-electronics, including electronic assays of membrane potential dynamics, nano-electronic actuation of cellular activity, and tomographic, nano-radar imaging of the morphology of vital organelles in the cytoplasm, during all phases of the cell life cycle (from development to senescence), under a variety of physiological environments, and under a broad suite of pharmacological manipulations. The interior of a vital, living cell contains multiple dynamic and electrically active organelles such as mitochondria, chloroplasts, and lysosomes. However, little is known about the detailed electrical activity inside the cell, in spite of well-recognized significance in biology and medicine. For example, the membrane potential of mitochondria "flickers" with a pattern that depends on organism age in model organisms such as C Elegans 1. Why does the dynamic electronic properties of this organelle relate to aging? In another example, the nano-scale morphology of mitochondria during apoptosis changes in a controversial way during chemotherapy and natural cell death 2. How does the mitochondrial morphology change during programmed cell death (apoptosis) 3,4 ? The key to answering these and other similar questions requires an electronic interface to vital, living cells in order to unlock the scientific mysteries and provide actionable medical treatments for many of the modern maladies plaguing human society such as aging, cancer, diabetes, and neuro-degenerative disorders, all of which are related