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How to comply with the regulatory requirements for manufacturing custom-made medical devices.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
How to conform with the legal requirements for placing medical devices on the market.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
What you need to do before your product can be placed on the Great Britain market with a UKCA mark.
How manufacturers can apply for approval to supply a non-compliant medical device on humanitarian grounds.
What you can do if your goods or vehicle are seized by Border Force or HM Revenue and Customs - get your things back or disagree with a customs seizure
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
When you do and do not have to offer a refund, repair or replacement, unconditional refunds for online purchases, and penalties for deceiving customers
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