MHRA and NICE Open Call for Evidence on Digital Mental Health Technologies Programme

Survey seeks stakeholder views on Phase 1 resources and their influence on knowledge, confidence, decision-making and practice.

The Medicines and Healthcare products Regulatory Agency (MHRA) and the National Institute for Health and Care Excellence (NICE) have launched a call for evidence to evaluate the impact of resources developed under the Wellcome-funded Digital Mental Health Technologies (DMHT) programme.

The survey opened on 5 November 2026 and will remain open until 26 February 2027. It is intended for a broad range of stakeholders, including developers and manufacturers of digital mental health technologies, healthcare professionals, researchers, policymakers, regulators, people with lived experience of mental health conditions, carers and members of the public.

Phase 1 evaluation

According to the MHRA and NICE, the survey forms part of the programme’s Phase 1 evaluation. It aims to assess how the resources have been received and used across the sector. The organisations are particularly interested in whether the materials have influenced users’ knowledge, confidence, decision-making and professional practice.

The resources were developed to support the safe development, regulation, evaluation and adoption of digital mental health technologies, including mental health apps and other digital tools. Findings from the survey will help determine whether the Phase 1 outputs have achieved their intended objectives and will inform the future direction of Phase 2 of the DMHT programme.

The MHRA and NICE encourage stakeholders to participate regardless of whether they have engaged extensively, minimally or not at all with the existing resources. The agencies say the feedback will help identify strengths, highlight areas for improvement and shape future work to improve the safety and effectiveness of digital mental health technologies.

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Talia Reiner

Talia Reiner covers power wheelchairs, hospital beds, patient lifts, and orthotic devices as a rehabilitation and home-care equipment analyst for institutional readers. Her assessments examine rated patient load, transfer geometry, battery runtime, serviceability, and care-setting fit against published specifications and maintenance requirements. She helps care-facility planners and home-care equipment buyers compare configuration, service coverage, and total cost of ownership while excluding individualized therapy and consumer shopping advice.