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Using an ecological momentary assessment to evaluate your digital health product.
How to use an interrupted time series to evaluate your digital health product.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Help your team understand why they need to meet the website and mobile app accessibility regulations.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Information on when software applications are considered to be a medical device and how they are regulated.
How to use routinely collected data to evaluate your digital health product.
Advice for manufacturers, members of the public and professional users of software or apps being used during the COVID-19 pandemic.
Download the NHS App, or open the NHS website in a web browser, to access a range of NHS services online.
How to use feedback from marketplace reviews to evaluate your digital health product.
How to use a crossover randomised controlled trial to evaluate your digital health product.
How to send information to Companies House through our extensible markup language (XML) schemas, by purchasing software or developing your own.
Practical steps to manage the risk of online harm if your online platform allows people to create anonymous or multiple accounts.
Information about how local authorities use open data to stimulate growth and innovation, save costs and develop more sustainable transport.
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