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How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Use form EXP-SAD/SEC (C88/ESS/LOI) with form C88/ESS where there is more than one item to declare.
Find out details of the Procedure Codes and Additional Procedure Codes (both Union and National) excluded from use with Simplified Declaration Procedure (SDP) with regular use and Entry in Declarants Records (EIDR).
Food and drink labelling and packaging regulations - what you must show, warnings, health and organic labels and packaging standards.
Advice and guidance on the health needs of migrant patients from Ecuador for healthcare practitioners.
Information on COVID-19, including guidance on the assessment and management of suspected UK cases.
Identify, describe, classify and manage waste upholstered domestic seating containing persistent organic pollutants (POPs).
Information on how UK companies can control risks when doing business in Mexico.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Get help to classify footwear and parts of footwear for import and export.
Find out if the goods you're declaring to inward or outward processing are classed as sensitive goods.
Check the tariff classification for preparations put up for retail sale.
FCDO travel advice for Ecuador. Includes safety and security, insurance, entry requirements and legal differences.
Advice and guidance on the health needs of migrant patients from Colombia for healthcare practitioners.
Guidance for industry on flexible approaches we are taking on good distribution practices.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Qualified Persons (QPs) should follow the below guidance on the flexible approaches we are taking for medicines imported from third countries.
Guidance on acetic acid (also known as ethanoic acid) for use in responding to chemical incidents.
Substances that are classed as persistent organic pollutants (POPs) and when you're allowed to use them.
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
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