handling into the eye. The cornea, which is the environment where the CL is worn, is the first layer of the eye to which we have direct access and plays an important role in monitoring the health of the ocular surface. A soft contact lens with graphenebased electrodes has been demonstrated to perform local electroretinogram which can monitor in real time the electrophysiology of the corneal surface. [8] Although, this device was tested in animal models, optical power correction (found in conventional contact lenses) was not included. Additionally, the parylene support layer in direct contact with the eye lid could introduce discomfort while blinking (since parylene is commonly known as hydrophobic). [9,10] Tear fluid, originated at the lacrimal gland and drained by the lacrimal ducts, [11] covers the corneal surface (for protection and moist) allowing the CL to float and at the same time to have a direct interaction with its physiology. [12] This thin fluid layer, divided in lipid (outer), aqueous (middle) and mucin (inner) containing all the physiologically active substances present in blood, [13] is commonly known as colorless and transparent blood. Different studies have been reported on the elucidation of the causal relationship between the presence (quantity/ frequency) of certain biomarkers (e.g., cancer biomarkers) and systemic diseases. [14,15] With this in mind, attempts to monitor the differentiation and abnormalities of systemic diseases have been actively researched in recent years by introducing a system capable of measuring a specific substance from within a contact lens, [16-20] or measuring a physical quantity (i.e., temperature, pressure, etc.). [21,22] Regarding biosensors focused on the tear fluid, different approaches have been demonstrated either embedded inside of a contact lens [4,23] or by means of an external device temporarily in contact with the tears. These techniques aim to develop noninvasive and continuous monitoring solutions. Although not inside a contact lens, a flexible and biocompatible amperometric glucose sensor in contact with the eye and with an external readout system was tested in animal models and compared with glucose levels measured in blood. [24] The results show a delay between 40 to 60 min after the oral administration of glucose, which could present a risk factor for patients in need of reliable and fast glucose measurements. In parallel, a glucose sensor Nowadays, smart contact lenses (SCLs) display interesting features for healthcare monitoring; however, their comfort and practical usability strongly depend on the outermost material in contact with the eye. In this publication, the embedding of a custom-made and thermoformed Near-Field Communication based circuit in a conventional soft CL is presented. The circuit is composed of gold tracks on polyimide between thermoplastic polyurethane layers (insert), while the lens is based on industry standard double-molding process of poly(2-hydroxyethyl methacrylate) with proven compatibility with corneal tissue. The lens ...