To build the best device possible we took a professional approach to our design and development processes.

User Based Approach

The L.A.S.S.O. is more than just the development of an idea; we wanted to see whether this device could be realistically implemented in practice. To create a product that had a future in a real-world situation, we decided it was vital to talk first to the people who would be using it: the patients and the CF healthcare team - people who understand the daily struggles and realities of treating cystic fibrosis. So we took a customer based approach by meeting with patients and medical staff to hear their view on how the L.A.S.S.O. should be designed to best meet their needs.

ISO Standards

After obtaining a clear direction for our device from potential users, we spoke to representatives from relevant industries. In particular we contacted a local company that developed medical equipment; the Institute of Medical Science and Technology. We were informed that the main body for devising procedures by which medical devices should be built is the International Organisation of Standards (ISO). As we live in a global community where such standards are important to ensure that “products and services are safe, reliable and of good quality”¹ there are strict procedures that must be adhered to. During the development of the L.A.S.S.O. we attempted to apply as many of the points given in the quality management standards 9001 and 13845 as we could. Standard 9001 dictates the procedures for general quality management; giving standards a company should follow when developing a product. Standard 13485 expands on 9001 to specify how a medical device should be developed. We followed these standards in the design and construction² of the L.A.S.S.O. wherever possible.

The ISO development criteria led to us completing a requirements document - documentation to show how we were meeting the users needs, the final aims of how the L.A.S.S.O. would operate and the functionality involved. Constructing the requirements documentation was an iterative process, updated after feedback from our supervisors, patients and medical staff. This iterative authoring process was again in line with protocol dictated by ISO standards.

The first iteration³ contains the version of the L.A.S.S.O. as if it were tested with The Lung Ranger detection component in place, which produces a bioluminescent output. The second iteration⁴ is a version informed by the audit that our L.A.S.S.O. underwent.