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Register to vote Register by 18 June to vote in the General Election on 4 July.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
Information about the EU Regulations and their implementation in Northern Ireland
Interested parties can review records of applications and statements submitted to OPRED as required by environmental regulations.
Use the pre-application advice service to find out the likelihood of getting a licence, what restrictions it may have and what you need to send with your application.
Get help to classify cigarettes, cigars, raw tobacco, smoking tobacco, tobacco for heating and nicotine substitutes for import and export.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Sets out process and expectations on pre-application discussions.
The New Active Substance Work Sharing Initiative (NASWSI) has successfully approved several medicines through this international collaboration and continues to foster cooperation and strong relationships between its Access partners. The Biosimilar Work Sharing Initiative (BSWSI) builds on this success.
Guidance on the 150-day assessment timeline for high-quality marketing authorisation applications including information on how to apply.
Apply for an import certificate to import a medicinal product into the UK for veterinary use.
These published standards relate to a number of KPIs in the VMD Deliverables and KPI document.
Explains planning controls relating to the storage of hazardous substances in England and how to handle development proposals around hazardous establishments.
Register as a manufacturer, importer or distributor of active substances.
You must get permission to export certain drugs and medicines.
Application form for getting an oil spill treatment product approved.
Supports effective delivery of planning application process.
Weights and Measures Act 1985 and subsequent Deregulation Order 1999 (as amended).
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.
How to apply to sell digital outcomes, specialists and user research services to government on the Digital Outcomes and Specialists framework.
How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application.
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