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Data, Freedom of Information releases and corporate reports
Spreadsheets are a common way to share data. Use this information to help you avoid common errors, improve interoperability and create more accessible spreadsheets.
Dstl ensures the UK can develop and exploit new sensor technologies for our defence and security, to find and assess potential threats and give information to decision-makers.
The characteristics, diagnosis, management, surveillance and epidemiology of Pseudomonas aeruginosa.
Dstl ensures the UK armed forces have the required weapons capability through research, development and demonstration of advances in science and technology.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Information and guidance on a range of medical devices for users and patients.
This guidance specifies the standards for the continuous monitoring and sampling of stack emissions.
Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
How to classify and describe your business waste so you can know how to manage and dispose of it - what you need to do, List of Waste (LoW) codes, technical guidance.
Information about the EU Regulations and their implementation in Northern Ireland
How to use a contextual inquiry when developing your digital health product.
Find data published by central government, local authorities and public bodies to help you build products and services.
Design, build and operate APIs in a consistent way
ARIA will focus on projects with potential to produce transformative technological change, or a paradigm shift in an area of science. ARIA is an executive non-departmental public body, sponsored by the Department for Science, Innovation and Technology .
How to use chatbots and webchat tools to improve your users’ experience of your service.
Guidance on the collection and reporting of data for CTAD, the surveillance system for all chlamydia tests done in England.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Work out your Statutory Adoption Leave dates - Ordinary and Additional Adoption Leave period, notice period and earliest start date
Project Orbis is a programme to review and approve promising cancer drugs helping patients access treatments faster.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
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