IEC 62083:2025 pdf download,Medical device software – Requirements for the safety of radiotherapy treatment planning systems.
IEC 62083:2025 establishes requirements for the design, manufacture, installation, and maintenance of radiotherapy treatment planning systems, covering both type tests and site tests.
The standard addresses these systems when they communicate with other medical devices, provided the systems:

Are used in medical practice;
Import data through operator input or from external devices;
Export data to other devices;
Are intended for routine operation under the supervision of qualified personnel by trained operators;
Are used and maintained according to the manufacturer’s instructions;
Operate within specified environmental conditions.

Furthermore, this document IEC 62083:2025 applies to any software application, whether standalone or integrated, that is employed for creating, assessing, or approving a treatment plan.