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Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
The duties and competence requirements for building regulations that clients, designers and contractors must meet.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Information about the EU Regulations and their implementation in Northern Ireland
Standardisation explained.
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Proposed updates to the lists of standards for businesses.
Guidance on certain consultation and publicity requirements of the Nationally Significant Infrastructure Project regime.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
What we require from each different type of landlord and the approach we will take
How RSH uses, and intends to use, its statutory regulatory and enforcement powers and certain general powers (from 1 April 2024)
Learn how the Government Digital Service is monitoring accessibility under the Public Sector Bodies (Websites and Mobile Applications) (No.2) Accessibility Regulations 2018.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Labelling rules for businesses in Great Britain (England, Scotland and Wales) and retailers in Northern Ireland, for certain agri-food products moved under the Northern Ireland Retail Movement Scheme.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
A Guide for Employers and Employees to the role of the Central Arbitration Committee (CAC) for these regulations
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
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