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A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Know which licence or certificate you must have to restrain, stun or kill animals which are not for human consumption, and how to carry out these operations.
Actions that trial sponsors should consider to build resilience into clinical trial design
A guide to documenting how you’ve collected your packaging data, known as your ‘methodology’. Online marketplaces affected by extended producer responsibility (EPR) for packaging must submit a methodology. This is also recommended for all producers as part of their ways...
How to use a factorial randomised controlled trial to evaluate your digital health product.
Information for patients, healthcare professionals and developers of new medicines
How to use a cost utility analysis to evaluate your digital health product.
This paper identifies a number of findings and recommendations in relation to the thematic areas of protracted crises, resilience, basic services and research uptake.
One hour GDS Academy online course on tools and techniques for leading interactive and engaging meetings in virtual rooms.
How the Industrial Emissions Best Available Technique (BAT) regime works from the end of the transition period.
How to use a before-and-after study to evaluate your digital health product.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Handling employees' grievances at work - setting up a grievance procedure, holding a grievance hearing and managing appeals
Information on Biosecurity Measures Plans, their importance, and why they are a requirement of Authorisation. Use this page to access standardised BMP modules.
Guidance on sexual transmission of Zika virus and methods of prevention.
Find out about partial exemption special methods for government departments.
A foreword on the Department for Levelling Up, Housing and Communities’ commitment to the evaluation of local growth programmes.
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