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How to use a quasi-experimental study to evaluate your digital health product.
How to use a before-and-after study to evaluate your digital health product.
Notices of publication and a consolidated list of references of pre-Exit European Assessment Documents for construction products.
RIDA funds research and development in new technologies, and new approaches to existing technologies, that support Sustainable Development Goals in south-east Asia.
A guide to collecting data about your packaging. This is for UK organisations affected by extended producer responsibility (EPR) for packaging.
Check the tariff classification for surface-active preparation for washing the skin and the hair (gel 2-in-1).
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.
Substances that are classed as persistent organic pollutants (POPs) and when you're allowed to use them.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Check the tariff classification for preparations put up for retail sale.
Find out how to make sure that data entered into the Customs Declaration Service (CDS) is matched correctly with the Automatic Licence Verification System (ALVS).
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Licence and registration application information for companies that deal in precursor chemicals.
Introducing the new pre-application service for Nationally Significant Infrastructure Projects.
Sets out process and expectations on pre-application discussions.
DECC Pre-Commercial Procurement Contract Template (Ref DPF31).
How to apply for simultaneous review of veterinary medicine submissions to the Australian Pesticides and Veterinary Medicines Authority (APVMA) and the VMD.
The process for the simultaneous review of veterinary drug submissions by Health Canada’s Veterinary Drugs Directorate and the UK's Veterinary Medicines Directorate.
The DUCR and the optional Part suffix is the main reference key to any Customs Handling of Import & Export Freight (CHIEF) declaration.
The process for the simultaneous review of veterinary medicine submissions by New Zealand’s Ministry for Primary Industries (MPI) and the UK's Veterinary Medicines Directorate.
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