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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.
Understand the challenges and considerations around using GraphQL such as security, versioning, caching, tooling and team skills.
How to prepare and what to do if you’re affected by extreme weather and natural hazards while travelling or living abroad.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to use a cost utility analysis to evaluate your digital health product.
Apply for the Registered Traveller service to get through UK border control faster and without filling in a landing card
How to use a cost benefit analysis to evaluate your digital health product.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
When and how to identify your kids and goats with tags.
Apply for a Temporary Work – Government Authorised Exchange (GAE) visa for work experience, training, research or fellowship - eligibility, extend or switch, family members
This guide sets out who has to apply for a permit, how to apply and explains the other rules covering travel to Antarctica.
Guidance for manufacturers, importers and distributors.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to use an N-of-1 study to evaluate your digital health product.
Guidance for living safely with respiratory infections, including coronavirus (COVID-19).
How to conform with the legal requirements for placing medical devices on the market.
Guidance for people with symptoms of a respiratory infection including COVID-19, or a positive test result for COVID-19.
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