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Register to vote Register by 18 June to vote in the General Election on 4 July.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
The duties and competence requirements for building regulations that clients, designers and contractors must meet.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
FCDO travel advice for Venezuela. Includes safety and security, insurance, entry requirements and legal differences.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
Apply for a Temporary Work – Government Authorised Exchange (GAE) visa for work experience, training, research or fellowship - eligibility, extend or switch, family members
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to meet the accommodation needs of guests, including information about gas safety and information about bills and paying rent.
Guidance on the pre-examination stage for Nationally Significant Infrastructure Projects.
Guidance on certain consultation and publicity requirements of the Nationally Significant Infrastructure Project regime.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Information about the EU Regulations and their implementation in Northern Ireland
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Licence and registration application information for companies that deal in precursor chemicals.
Advice for manufacturers of Class I medical devices for placing products on the UK market
Information and resources for developers about broadband infrastructure and connectivity requirements for new homes.
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