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Register to vote Register by 18 June to vote in the General Election on 4 July.
Chargepoint and infrastructure specifications and claim guidance for electric vehicle chargepoint and infrastructure grants.
A form of IP that extends the protection of patented active ingredients present in pharmaceutical or plant protection products.
This guidance summarises the types of defects to which the leaseholder protections in the Building Safety Act 2022 apply.
This guidance sets out further information about what you, the leaseholder, do and do not have to pay for remediating a building safety defect via your service charge.
We are allowing alternative courses of actions for manufacturing or laboratory equipment during the outbreak.
Divisional letter dated 8 December 2010 about designated warranty scheme by Construction Register Ltd
What to do if your vehicle, vehicle part or accessory is recalled, has a registered fault and how to report serious safety defect you find
Guidance for businesses.
Producer responsibility laws in the UK cover packaging, electrical and electronic equipment (EEE), batteries and end of life vehicles (ELVs).
Use form LL AA06 as a statement of guarantee for a subsidiary limited liability partnership (LLP).
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
This order requires retailers of domestic electrical goods to make the prices and terms of their extended warranties clear.
Guidance on applications and licences for manufacturers & wholesalers, suspended and revoked licences, registrations, exporting medicines, defective medicinal products and fees.
Forms to make a variation to a manufacturer's licence.
How to make sure your business’ terms and conditions are fair, and avoid unfair contract terms
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
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.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
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