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List of controlled goods that follow the normal import declaration rules if HMRC apply continuity plans due to system issues.
Pharmacovigilance system requirements
Annex VII information accompanying shipments of waste as referred to in article 3(2) and 3(4).
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How a marketing authorisation holder should report a defect with a veterinary medicine.
Permitted descriptions for gold plated silver articles at point of sale in the UK.
Industry must notify the MHRA if they will not be using these flexibilities
Use these general provisions to help you determine the origin of your products.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
Substances that are classed as persistent organic pollutants (POPs) and when you're allowed to use them.
To help you protect, manage and enforce your intellectual property (IP) rights in Philippines.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
This page contains the articles of association you will need if you are setting up a Community Interest Company (CIC) that is limited by shares.
This research applies to low-income and middle-income countries in the Eastern Mediterranean Region
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.
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