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Register to vote Register by 18 June to vote in the General Election on 4 July.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
When HMRC will issue a joint and several liability notice to individuals who have been involved with companies which have become insolvent and have a tax liability with HMRC.
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
Marking, labelling and marketing standards you must follow to import and export plant seeds, food and manufactured goods.
Steps to help grow your business - finding finance, mentors, increasing sales and developing products and services
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
How to market eggs, including rules on registration, egg marking, salmonella control and egg marketing inspections in England and Wales.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Guidance for suppliers and dealers.
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.
How to use a multiphase optimisation strategy (MOST) to evaluate your digital health product.
The CMA has today published its main concerns following an initial review into the veterinary sector.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
Submissions related to human medicines need to be submitted directly to the MHRA.
Guidance for the pharmaceutical industry on how to apply for an authorisation to place a veterinary medicine on the UK market or part of, or to expire one.
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