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1642217
registered interest false more like this
date remove maximum value filtermore like thismore than 2023-06-06
answering body
Department of Health and Social Care more like this
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care more like this
hansard heading Cannabis: Medical Treatments remove filter
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Health and Social Care, what steps his Department is taking to ensure the (a) quality and (b) safety of imported cannabis-based products for medicinal use; if he will make a statement. more like this
tabling member constituency North Herefordshire more like this
tabling member printed
Sir Bill Wiggin more like this
uin 187907 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2023-06-14more like thismore than 2023-06-14
answer text <p>Cannabis based products for medicinal use in humans (CBPMs) is a term that usually designates medicinal products that are not licensed in the United Kingdom. Most CBPMs in use in the UK are unlicensed medicines imported into the Country. Regulation 167 of the Human Medicine Regulations 2012, as amended, allows for medicines without a marketing authorisation, also referred to as a licence, to be supplied under certain circumstances. In the interest of public health, the exemption is narrowly drawn because unlicensed medicines or specials, unlike licensed medicinal products, have not been assessed by the Licensing Authority against the criteria of safety, quality and efficacy.</p><p>An unlicensed medicine may be supplied following a bona fide unsolicited order and is formulated in accordance with the specific requirements of the prescriber. This means that the quality, safety and efficacy of unlicensed medicines is the direct responsibility of the prescribers responsible for the care of individual patients as they are the ones that determine if these are fit for purpose.</p><p>The Medicines and Healthcare products Regulatory Agency (MHRA) ensures that any importer of an unlicensed medicinal product into the UK must be suitably licensed to import unlicensed medicines and prior to the importation taking place the importer must notify of their intent to import the unlicensed medicine and provide a set of supportive documentation, which the MHRA will assess to ensure the medicine’s quality and safety. This typically includes the requirement that a medicine has been produced in facilities meeting Good Manufacturing Practice or equivalent recognised quality standards for medicines.</p>
answering member constituency Colchester more like this
answering member printed Will Quince more like this
question first answered
remove filter
answering member
4423
label Biography information for Will Quince more like this
tabling member
1428
label Biography information for Sir Bill Wiggin more like this