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How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
A research project to strengthen the Government Chemist capabilities for the analysis of vitamins.
Find a supplier who can provide a user research studio through the Digital Outcomes and Specialists framework.
How to use interviews to evaluate your digital health product.
How to take part in user research at the UK IPO – signing up, who we want to meet with, why we research and your data rights.
How to use a contextual inquiry when developing your digital health product.
OPSS would like to invite any interested parties, to submit any scientific information relevant to the safety assessment of nanomaterials used in cosmetics.
How to use a feasibility study when planning the evaluation of your digital health product.
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 .
Compare different evaluation approaches and choose an appropriate method.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to write up and share your findings
Find a supplier who can provide user research participants to test your service with.
The Vaccine Development Evaluation Centre (VDEC) at Porton Down in Wiltshire facilitates the development and evaluation of new vaccines and therapeutics.
The agreement for a first-of-a-kind test rig will provide critical data for the design and development of Spherical Tokamak for Energy Production (STEP).
OPSS would like to invite any interested parties to submit any scientific information relevant to the safety assessment of cosmetic ingredients.
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