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Get help to classify footwear and parts of footwear for import and export.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
International co-operation for export credit financing, how UK Export Finance works with the OECD, the EU, the Paris Club and the Berne Union.
Information for manufacturers.
A guide to collecting data about your packaging. This is for UK organisations affected by extended producer responsibility (EPR) for packaging.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Protocols and procedures for testing the value for cultivation or use (VCU) of agricultural crops.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Find out how to make sure that data entered into the Customs Declaration Service (CDS) is matched correctly with the Automatic Licence Verification System (ALVS).
Use this form to respond to an application for the extension of pre-charge bail.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Obligated packaging producers must register and meet their waste packaging recycling responsibilities.
Find out about exporting products of animal origin (POAO) such as meat, dairy and fish, live animals, plants and plant products.
Check the tariff classification for antimicrobial bathing systems.
How to apply for simultaneous review of veterinary medicine submissions to the Australian Pesticides and Veterinary Medicines Authority (APVMA) and the VMD.
How catch limits are set and how to get involved in setting them. This includes current catch limits and closed fishing areas.
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
Working with contract management and accreditation.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
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