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Register to vote Register by 18 June to vote in the General Election on 4 July.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Rules covering how entertainment and modelling agencies work; charging fees and refunds for for finding work
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
The Valuation Office Agency (VOA) asks for rental and lease information to assess the rateable value of non-domestic properties.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
How to market eggs, including rules on registration, egg marking, salmonella control and egg marketing inspections in England and Wales.
This collection brings together documents related to the government's work to combat domestic and international corruption.
This guidance aims to help tutoring services to comply with the requirements of the Employment Agencies Act 1973 (the Act) and Conduct of Employment Agencies and Employment Businesses Regulations 2003 (the Conduct Regulations).
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Details of the Yellow Card scheme, which is the system for recording adverse incidents with medicines and medical devices in the UK.
Employers' responsibilities for different contract types: full-time, part-time, fixed term, agency workers, consultants, zero hours, family members, volunteers and young workers
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
How the Valuation Office Agency calculates your rateable value for business rates.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
How to contact MHRA for specific services or enquiries.
How to renew marketing authorisations for products granted through different routes and at different times.
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