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Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
This guidance explains what rules of origin (RoOs) are and the changes under the Developing Countries Trading Scheme (DCTS).
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
Licence and registration application information for companies that deal in precursor chemicals.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Information for companies on the import and export of controlled drugs to and from the UK.
How to get and maintain an ATT qualification, and what to do if you want to end your authorisation.
Guidance for hospitals, tissue establishments and fertility clinics for ensuring the quality and safety of human organs, tissues and cells (including reproductive cells).
Information on taking, submitting and processing samples which potentially contain MPXV.
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