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<p>In February 2019, the then Home Secretary commissioned the ACMD to conduct a longer-term
review of Cannabis-Based Products for Medicinal use (CBPM). The ACMD published their
report on 27 November 2020 on gov.uk. In it they recommended:</p><p><em>“that the
scheduling of CBPMs under Schedule 2 of the MDR remains appropriate and that no further
legislative amendments to the MDR regarding CBPMs are required at this point in time.”</em></p><p>Unlike
Sativex, most CBPM do not have a marketing authorisation from the Medicines and Healthcare
products Regulatory Agency (MHRA). As such, in the absence of the reassurance that
a CBPM has gone through the safety, quality and efficacy process established by the
MHRA, it is right that it is in Schedule 2 of the Misuse of Drugs Regulations 2001.
However, should a cannabis-based medicine receive a marketing authorisation from the
MHRA, the Government will commission the Advisory Council on the Misuse of Drugs (ACMD)
to reconsider the scheduling of the product under the Misuse of Drugs Regulations
2001. This was the case for Sativex following its marketing authorisation.</p>
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