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Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Find the address, contact details and opening times of the UK visa application centre for your country.
Pharmacovigilance system requirements
Information on UK sanctions currently in place and how to apply for the appropriate licences.
Make sure that domains that do not send email cannot be used for spoofing.
Check the tariff classification for dried buffalo ears and dried beef meat scraped off from the throat, for use as animal feed.
Listing of countries with a known occurrence of high consequence infectious disease (HCID).
Helping public health practitioners conducting evaluations on how to plan them.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Find out which birds and animals may be spared from culling during an outbreak of an exotic animal disease.
The signs of swine vesicular disease, what to do if you suspect it in your animals and measures to prevent its spread.
The Board was responsible for safeguarding and advancing public health by assuring the quality and safety of biologicals, through its management of the National Institute for Biological Standards and Control (NIBSC). In July 2008 the Health and Social Care Act...
Guidance for those producing, processing, consuming, importing or exporting chemicals covered by the Chemical Weapons Convention (CWC)
Paper and cardboard production can cause significant pollution. This guide describes industry responsibilities for preventing pollution.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
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.
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
Nigeria is subject to regional controls governing small arms and light weapons.
The requirements for packaging DNLEU
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