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If you put EEE on the UK market you must follow rules on both the EEE you sell and the EEE that becomes waste (WEEE).
Guidance on applying to renew a marketing authorisation (MA) for a veterinary medicine.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Employers' responsibilities when using agencies to find staff, including health and safety, access to facilities, vacancies, continuous employment, transfer fees and complaints
Rules covering how entertainment and modelling agencies work; charging fees and refunds for for finding work
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
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.
How to apply for marketing authorisation via this new procedure.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
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.
UKHSA Chief Executive Professor Dame Jenny Harries visits Manchester and Liverpool to launch campaign as measles cases continue to rise.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
How to market eggs, including rules on registration, egg marking, salmonella control and egg marketing inspections in England and Wales.
The Valuation Office Agency (VOA) asks for rental and lease information to assess the rateable value of non-domestic properties.
This collection brings together documents related to the government's work to combat domestic and international corruption.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
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 .
Employers' responsibilities for different contract types: full-time, part-time, fixed term, agency workers, consultants, zero hours, family members, volunteers and young workers
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