A bill of materials may list every component on a board and still leave questions that prevent a manufacturing quotation from being prepared. A manufacturer part number is missing, two positions have conflicting descriptions, or it is unclear which components…
The manufacturing of PCBs for medical devices is subject to much stricter regulatory requirements than those in other electronics sectors. ISO 13485 certification establishes the framework for ensuring the safety, traceability, and quality of medical devices throughout their entire lifecycle…
The use of flexible, multilayer PCBs is one of the technical consequences of the evolution of advanced medical devices; that is, portable, implantable, and with complex geometries. The main outcome of these technologies is the integration of high-performance electronics…