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Register to vote Register by 18 June to vote in the General Election on 4 July.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
How to market forest reproductive material (FRM) for forestry purposes, including regulations, registration, master certificates and licences.
Marking, labelling and marketing standards you must follow to import and export plant seeds, food and manufactured goods.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How the MHRA processes variations to Marketing Authorisations (MAs)
How to renew marketing authorisations for products granted through different routes and at different times.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
Don’t include personal or financial information like your National Insurance number or credit card details.
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