What do you ultimately want to achieve?
Identify and qualify Second Source Materials
Second source materials from alternative adhesive suppliers should not only meet the required quality and regulatory standards, but also ensure the end user does not perceive any difference in the device.
This type of project involves identifying and qualifying alternative suppliers for key adhesive materials and components to ensure there are no disruptions in the production process. Often, it is critical that the end user does not perceive any visible or palpable difference in the device, despite using raw materials from multiple sources.
This process usually starts with a thorough evaluation of various samples to test if the alternative adhesive materials represent a viable second source option, while also ensuring they meet the stringent quality and regulatory standards necessary for medical devices. Crucial in this development process is to successfully identify the attributes of the current raw materials that must be present in the second source materials.
Once those inputs are understood, the development process to design a new product is initiated. In response to market and users' needs, Avery Dennison Medical offers a wide array of standard adhesive and substrate options, and also supports the development of customized solutions.