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Explains planning controls relating to the storage of hazardous substances in England and how to handle development proposals around hazardous establishments.
Customer declaration of specific uses of the scheduled category 1 or 2 substances (individual transactions).
Substances that are classed as persistent organic pollutants (POPs) and when you're allowed to use them.
Get help to classify organic chemicals that contain certain permitted additives or can be dissolved in water, for import and export.
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.
Licence and registration application information for companies that deal in precursor chemicals.
When a material is waste, is a by-product or meets ‘end of waste’ status.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
How to carry out a risk assessment if you are applying for a bespoke permit that includes discharging hazardous chemicals and elements to surface water.
Customer declaration of specific uses of the scheduled category 1 or 2 substances (multiple transactions).
How to comply with the exemption from the Veterinary Medicines Regulations that allow certain animal medicines to be sold without a marketing authorisation.
How product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
Register as a manufacturer, importer or distributor of active substances for use in veterinary medicines.
Guidance for those producing, processing, consuming, importing or exporting chemicals covered by the Chemical Weapons Convention (CWC)
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Guidance on the European Union regulation on explosives precursors, including licensing, labelling and reporting suspicious activity
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
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