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Provides advice on the key points to take into account on design.
A list of 10 criteria that represent good practice in creating, applying and enforcing design codes.
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
The duties and competence requirements for building regulations that clients, designers and contractors must meet.
The UK government's design principles and examples of how they've been used.
How to use a quasi-experimental study to evaluate your digital health product.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Outline of the design approach taken to various aspects of the baseline designs
Essential resources for project delivery professionals leading, managing or involved in projects or programmes in government.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Tools to support the design and assess the quality of active travel interventions and schemes.
Find out how new woodland can enhance landscape character as well as a wide range of benefits to the woodland owner and society.
The information clients, principal designers, principal contractors and accountable persons need to keep.
The shape and the configuration of objects are automatically protected by design right in the UK and Europe.
Register a design - what designs are protected, search the registers, prepare your illustrations, how to apply, disclaimers and limitations.
Guidance relating to the protection, managing and enforcing of a registered design. Registered designs protect the appearance, shape or decoration of a product.
Find registered designs in the UK
View designs registered in the designs journal from the last 25 years
This page provides a guide for those interested in key upcoming digital regulatory activity being explored, developed or implemented by government. It covers a range of governance activities, from legislative change to the development of co-regulatory and self-regulatory frameworks.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
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