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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.
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Get information on teacher training courses, funding, pay scales and how to make a great application
Pharmacovigilance system requirements
How investigators and sponsors should manage clinical trials during COVID-19
Marburg virus is a Filovirus which, along with Ebola virus, can cause a severe and often fatal viral haemorrhagic fever (VHF).
Check how much your visa application costs in the country you’re in
This document explains: how patients are tested and treated, and steps in place to prevent its spread.
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...
Make sure that domains that do not send email cannot be used for spoofing.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
Helping public health practitioners conducting evaluations on how to plan them.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
Information about the EU Regulations and their implementation in Northern Ireland
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
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
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