My activity
- Last accessed:
- Current status:
-
Course Information
- Title:
- For general public
- Description:
-
This course has 2 tip sheets:
Public tipsheet 1: Regulation and evaluation of digital mental health technologies: This tip sheet explains the role of the Medicines and Healthcare products Regulatory Agency (MHRA), defines DMHT and focuses on steps 1 to 5 of the 7 steps to reviewing the intended purpose, safety and evidence of the product and its appropriate regulation.
Public tipsheet 2: Safety of digital mental health technologies: This tip sheet is to help you understand how the safety and performance of DMHTs are monitored. This includes how to report concerns when the use of the product has contributed to an adverse incident. - Hierarchy:
- MindEd Medicines and Healthcare Products Regulatory Agency (MHRA): Digital Mental Health Technologies (DMHT) > For general public
- Keywords:
- Medicines and Healthcare products Regulatory Agency, MHRA, Digital Mental Health Technologies, DMHT, SaMD, Software as a medical device, Medical Device, intended purpose, safety, regulation, regulatory status, risk, Class of medical devices, UKCA marks, CE marks, registration, medical purpose, NICE, yellow card scheme, yellow card, MHRA medical vigilance system, adverse events, serious incidents
- Created:
- 5 Jan 2026
- Updated:
- 5 Jan 2026
Share this item
- Copy URL
- Title:
- For general public
- Description:
-
This course has 2 tip sheets:
Public tipsheet 1: Regulation and evaluation of digital mental health technologies: This tip sheet explains the role of the Medicines and Healthcare products Regulatory Agency (MHRA), defines DMHT and focuses on steps 1 to 5 of the 7 steps to reviewing the intended purpose, safety and evidence of the product and its appropriate regulation.
Public tipsheet 2: Safety of digital mental health technologies: This tip sheet is to help you understand how the safety and performance of DMHTs are monitored. This includes how to report concerns when the use of the product has contributed to an adverse incident. - Hierarchy:
- MindEd Medicines and Healthcare Products Regulatory Agency (MHRA): Digital Mental Health Technologies (DMHT) > For general public
- Keywords:
- Medicines and Healthcare products Regulatory Agency, MHRA, Digital Mental Health Technologies, DMHT, SaMD, Software as a medical device, Medical Device, intended purpose, safety, regulation, regulatory status, risk, Class of medical devices, UKCA marks, CE marks, registration, medical purpose, NICE, yellow card scheme, yellow card, MHRA medical vigilance system, adverse events, serious incidents
- Created:
- 5 Jan 2026
- Updated:
- 5 Jan 2026