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Register to vote Register by 18 June to vote in the General Election on 4 July.
Guidance for hospitals, tissue establishments and fertility clinics for ensuring the quality and safety of human organs, tissues and cells (including reproductive cells).
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
What blood establishments, blood banks and manufacturers of blood products need to do to ensure the safety and quality of blood and blood products.
How to use a cost utility analysis to evaluate your digital health product.
Guidance on the Quality Matters initiative, which aims to improve the quality of adult social care.
Pharmacovigilance system requirements
The Commission on Human Medicines (CHM) advises ministers on the safety, efficacy and quality of medicinal products. CHM is an advisory non-departmental public body, sponsored by the Department of Health and Social Care .
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
The government is committed to improving the quality of social housing in England. In response to the tragic death of 2-year-old Awaab Ishak, we are reforming the sector so that every tenant has a decent, safe and secure home. We report...
A guide to human behaviour in the shipping industry.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
Government response to the report on: ‘Supporting progression out of low pay: a call to action’.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Helping public health practitioners conducting evaluations – choosing evaluation methods.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Information about ensuring blood and blood component safety.
When a material is waste, is a by-product or meets ‘end of waste’ status.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
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