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Pharmacovigilance system requirements
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
What you need to do to work and operate in the aviation industry.
AVU provides services for genotypic antiviral resistance testing of HIV and HCV, investigation of HIV transmission events and HSV antiviral resistance testing by phenotyping.
The Civil Aviation Authority (CAA) is responsible for the regulation of aviation safety in the UK, determining policy for the use of airspace, the economic regulation of Heathrow, Gatwick and Stansted airports, the licensing and financial fitness of airlines and...
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Development of a standard approach for AI and autonomy in networked multi-sensor systems in security and defence.
UK Health Security Agency's laboratories provide a comprehensive range of microbiological tests and services.
Defence Standardization develops and pursues MOD’s standardization policy, both nationally and internationally, with civil and military partners to support increased interoperability and more effective acquisition.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Nigeria is subject to regional controls governing small arms and light weapons.
Check the tariff classification for articles made of cermet.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Check the tariff classification for the unassembled parts to be implanted into the human body for different spinal treatments.
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
This guidance specifies the standards for the continuous monitoring and sampling of stack emissions.
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