October 28, 2022

What is Software As a Medical Device?

Software will dominate the medical device market in the near future as technology develops and becomes more and more embedded in digital platforms, where its applications in the healthcare and medical sectors are particularly prominent.

The IMDFR defined SaMD as a “software intended to be used for one or more medical purposes that perform these purposes without being part of a hardware medical device”.

There are three types of software related to medical devices

  • Software as Medical Device (SaMD)
  • Software that is integral to a Medical Device
  • Software used in the manufacture or maintenance of Medical Device

Examples of SaMD:

  • Software that allows a mobile device to view images from an MRI, ultrasound, or X-ray that are used for diagnostic purposes
  • Software that processes images which help to detect breast cancer

Classification of SaMD:
SaMD is categorized into class I to IV based on the levels of impact on the patient or public health and also the level of risk with class I represent the low risk and class IV with high risk.

General Considerations for SaMD:

IEC 62304 is a standard for life-cycle development of medical device software. The standard specifies a risk-based decision model, defines some testing requirements, and highlights three major principles that promote safety relevant to SaMD.

Other Resources
Uncategorized

Digital Health The categories of digital health include mobile health (mHealth), Health Information technology (IT), wearable devices, telemedicine, telehealth and personal medicine. Digital health has the potential to improve the ability to accurately diagnose and treat diseases which enhances the delivery of health care for the individual. The applications of these technologies range from general […]


January 26, 2023 | 4 mins Read
Regulatory compliance

National Medical Products Administration (NMPA) is responsible for the regulation of Medical devices and Pharmaceuticals in China. The predecessor to NMPA was founded in 1998, and renamed as State Food and Drug Administration in 2003. On September 1, 2018 China Food and Drug Administration was replaced by NMPA and it operates under the state jurisdiction […]


November 22, 2022 | 4 mins Read
Regulatory compliance

In today’s world of healthcare, technology plays an important role in the life cycle of medical devices and software has become an integral part of majority of products that serve both medical and non medical purposes. There are three types of medical devices related to software. Namely, Software as a Medical Device (SaMD), Software in […]


November 13, 2022 | 4 mins Read

Hop on this transformational journey with us.

Contact Us