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Register to vote Register by 18 June to vote in the General Election on 4 July.
How to determine meaningful findings from your observations of user research.
This series brings together all documents relating to referee analysis carried out under the Government Chemist statutory function.
Reports and data on export control licensing compiled by the export control organisation.
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to use an N-of-1 study to evaluate your digital health product.
You can use a SIEL to make shipments of specified military or dual-use items to a named consignee and/or end user.
Formerly part of M18, how to prepare and interpret analytical quality control (AQC) charts to verify the performance of your monitoring method.
Helping public health practitioners conducting evaluations – choosing evaluation methods.
How to use a crossover randomised controlled trial to evaluate your digital health product.
This guidance explains what rules of origin (RoOs) are and the changes under the Developing Countries Trading Scheme (DCTS).
Check what side effects people have reported when they've taken a medicine.
How to carry out a risk assessment if you are applying for a bespoke permit that includes discharging hazardous chemicals and elements to surface water.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to assess a planning application when there are invertebrates on or near a proposed development site.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
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