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Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
Find out how to link your temporary storage facility to Customs Handling of Import and Export Freight (CHIEF) or the Customs Declaration Service using a Community Systems Provider.
Guidance for those producing, processing, consuming, importing or exporting chemicals covered by the Chemical Weapons Convention (CWC)
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Protocols and procedures for testing the distinctiveness, uniformity and stability (DUS) of certain agricultural and vegetable plants.
Owners and vets can use this form to confirm an XL Bully dog has been neutered.
Publish your code and use open source to improve transparency, flexibility and accountability.
Information to help you protect, manage and enforce your intellectual property (IP) rights in the European Union and the European Economic Area (EEA).
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
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
You can use a SIEL to make shipments of specified military or dual-use items to a named consignee and/or end user.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
Check if you need a visa or permit to work in France and how to get one if you do.
Advice for medical professionals to follow when assessing drivers with neurological disorders.
Diseases and health problems in sheep and goats, including foot and mouth disease (FMD), scrapie and lead poisoning
Find details of recent trade mark applications or amendments by searching the journal
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
Guidance for industry on flexible approaches we are taking on good distribution practices.
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