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Register to vote Register by 18 June to vote in the General Election on 4 July.
The Criminal Cases Unit is responsible for the assessing all special preparation claims under the litigator graduated fee scheme and advocates graduated fee scheme.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
To support teachers in making early years foundation stage profile (EYFSP) judgements.
Food and drink labelling and packaging regulations - what you must show, warnings, health and organic labels and packaging standards.
These documents are for the use of individuals who are the subject of an application to retain DNA profile and/or fingerprint records.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Guidelines on the prosecutor’s role in applications for Witness Anonymity Orders: Criminal Evidence (Witness Anonymity) Act 2008.
Accessible documents at the Adjudicator’s Office
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 to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to make sure you take reasonable care if you need to send tax returns and other documents to HMRC, and what happens if you do not.
Packaging regulations: environmental requirements, recycling
Find out how to submit your research to Athena, Dstl's central repository of MOD-sponsored scientific and technical research reports.
A guide to documenting how you’ve collected your packaging data, known as your ‘methodology’. Online marketplaces affected by extended producer responsibility (EPR) for packaging must submit a methodology. This is also recommended for all producers as part of their ways...
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Pharmacovigilance system requirements
Documents, certificates, letters and notes available at the British Embassy Podgorica.
A protocol on the use of casework material for validation purposes.
A collection of guidance, news articles and promotional material for the DBS Update Service.
Don’t include personal or financial information like your National Insurance number or credit card details.
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