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Data, Freedom of Information releases and corporate reports
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
Apply for a higher education course, track your application and accept or reject your offers.
Details of General Licences issued by OFSI
Find registered patents, patent applications and pending patents
Get information on teacher training courses, funding, pay scales and how to make a great application
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.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Pharmacovigilance system requirements
How to object to the registration of a lasting or enduring power of attorney - including forms and fees
The Intellectual Property Office (IPO) is the official UK government body responsible for intellectual property (IP) rights including patents, designs, trade marks and copyright. IPO is an executive agency, sponsored by the Department for Science, Innovation and Technology , supported...
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Make sure that domains that do not send email cannot be used for spoofing.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
Check how much your visa application costs in the country you’re in
Information and advice on rabies, the viral infection of the central nervous system which affects mammals and humans.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
Apply for a Secondment Worker visa to work for a UK organisation as part of a high-value contract - eligibility, fees, documents, extend, switch or update, bring your partner and children.
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