The Intrepid Clinical Engineering Study

The purpose of this research study is to collect clinical data to validate a software update for 12-lead electrocardiogram monitoring.

Inclusion Criteria: * Able to read, write, speak, and understand English * Age: 29 days to 89 years * Willing and able to provide informed consent and complete study procedures * Willing to have Philips representatives present during study procedures. Exclusion Criteria: * Known allergy to medical adhesives, silicone, or latex (per self-report) * Any limitation or medical condition, including but not limited to physical or cognitive disability, that would affect the participant's ability to complete study activities (per investigator) * At the time of enrollment, current enrollment in any other interventional research study * An employee, or residing family member of an employee, of a company that designs, sells, or manufactures monitor/defibrillator technology or related products (including Philips)