Medical software development needs to be foolproof as this industry cannot afford mistakes. Hence, during the development of such products, developers follow a process to ensure that the product is safe for use and functions efficiently.
For example, if a brand launches supplements, they have to be approved by the Food and Drug Administration (FDA) to get their product in the market. FDA sets these standards for quality system regulation. The same goes for digital products; there are five phases of medical software development.
- Initiation and risk analysis
It is the first phase where ideas are documented. After documentation, people estimate how much resources will be needed throughout the software developments process. Next, developers need to ensure whether this software would be worth developing or not at the very first stage.
They can do that by comparing the main objective behind the prospective software and the goals behind all medical software development. If they benefit the well-being of patients or help healthcare professionals, then only it’ll be worth it. People also measure the risks involved during initiation.
- Formulation and Concept
During this stage, you prove that your idea is worth the efforts and resources being spent on it; hence it is critical. The medical software built should be feasible, efficient, and financially affordable for the target audience. For this, you need to conduct research and back up your ideas with facts and figures.
