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The Fund aims to create the opportunity to build strong partnerships between UK and Turkish scientists, researchers and institutions.
Apply for a licence to move and keep certain non-native (alien) species for animal welfare purposes.
Get help to classify articles of leather and other items in chapter 42 of the tariff for import and export.
Marburg virus is a Filovirus which, along with Ebola virus, can cause a severe and often fatal viral haemorrhagic fever (VHF).
Apply for an International Sportsperson visa if you're an elite sportsperson or coach with sponsorship - getting sponsored, eligibility, documents, extend your visa, family members
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
The epidemiology, symptoms, diagnosis and management of human T-cell lymphotropic virus types 1 and 2 (HTLV-1 and HTLV-2).
Free support and advice if you've been the victim of crime and information on restorative justice.
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
Use this form to change the location of a limited liability partnership's (LLP) records to its registered office.
You may be able to get provisional entitlement to higher category vehicles, and automatic entitlement to lower categories if you pass a higher category driving test.
How investigators and sponsors should manage clinical trials during COVID-19
Use form LL VT01 to certify voluntary translation of a document for a limited liability partnership (LLP) in English.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Garth is a men’s high security prison near Leyland, Lancashire.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Examples of how and when to adjust the customs value for commercial level and quantity when using Methods 2 or 3 if you’re an importer or clearing agent.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
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