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Register to vote Register by 18 June to vote in the General Election on 4 July.
Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
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.
Competent authorities of exporting countries should use the relevant model health certificate as a template to create a version exporters can apply for to export gelatine and collagen intended for human consumption to Great Britain, the Channel Islands or Isle...
Form CH10: Order for an injunction (intended action).
Find out which gas appliances must comply with the Gas Appliances (Safety) Regulations 1995, exemption and penalties for non-compliance
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Customers must no longer access programmes via EU satellite broadcasting services to avoid a charge for a UK service.
The external quality assessment (EQA) Legionella isolation scheme is suitable for laboratories that examine waters for Legionella spp.
How to get fast-track approval of medical devices during COVID-19.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
This external quality assessment (EQA) scheme is suited for laboratories that test food for Staphylococcus aureus enterotoxin (SET) using a range of kits.
Use this form to apply for an order preventing any transactions intended to defeat a claim for financial relief by the applicant.
This scheme is for laboratories in the water testing and clinical microbiology sectors that monitor the microbial quality of water-used rinse endoscopes.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
When and how to identify your kids and goats with tags.
Competent authorities of exporting countries should use the relevant model health certificate as a template to create a version exporters can apply for to export other animal by-products to Great Britain, the Channel Islands or Isle of Man.
Advice for manufacturers of Class I medical devices for placing products on the UK market
When and how to identify your lambs and sheep with tags.
The UK's regulatory framework for strategic export controls and the circumstances where you might need an export licence.
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