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How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How investigators and sponsors should manage clinical trials during COVID-19
These guidelines give commissioners, providers and healthcare professionals in cancer screening information on consent to screening and procedures.
Risk assessment methodology to support decisions on red list countries and territories.
New age ratings to be introduced on Relationships, Sex and Health Education content in schools to ensure it is appropriately and sensitively taught.
Sets out key principles in understanding viability in plan making and decision taking.
This report describes the approach that the mentorship programme for beneficiary institutions in Zimbabwe will take
If you're registered for the VAT Import One Stop Shop (IOSS) in the EU and sell eligible low value goods into Northern Ireland, use this service to tell HMRC your VAT IOSS registration number.
The What Works Network uses evidence to improve the design and delivery of public services.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Capacity building activities to equip policy makers with the relevant skills to access, evaluate and use research evidence
If you hold certain information, you should contact OFSI as soon as practicable.
Lessons from mining and forestry and their implications for REDD+
How end-use controls apply to weapons of mass destruction (WMD) related goods, software, technology and technical assistance.
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