My Lords, I too thank the Minister for her explanation of the content and purpose of the draft order, which we do not oppose. It amends the Misuse of Drugs Act by narrowing the previous definition of synthetic cannabinoids, as the previous definition has had the effect of requiring compounds that are not of concern to be licensed as class B drugs.
Following the control of the first generation of synthetic cannabinoids in 2009 and of the second generation in 2013, the Advisory Council on the Misuse of Drugs first published advice in 2014 on the third generation of synthetic cannabinoids—a group of compounds commonly referred to, as the Minister said, as Spice and Mamba, which mimic the effects of cannabis. The ACMD recommended that these compounds be captured by way of a generic definition as class B drugs under the Misuse of Drugs Act. It also recommended that the compounds be placed in Schedule 1 to the Misuse of Drugs Regulations 2001, meaning that they can be legally accessed only with a Home Office licence, which is generally issued for research or industrial purposes.
Following the ACMD’s recommendations, the changes came into effect on 14 December 2016 but, as has already been said, shortly after their implementation the ACMD and the Home Office were told by research bodies that the breadth of the definition meant that it captured a large number of research compounds, many of which were not synthetic cannabinoids. The effect of this was that research institutions had to obtain Schedule 1 licences when they should not have needed to do so.
The ACMD recognised that its advice that led to the 2016 changes had unintended consequences. As a result, it made a further recommendation in December 2017 to the effect that the scope of the generic definition be reduced. Accordingly, this order amends the generic definition of third-generation synthetic cannabinoids by replacing the term “univalent” with a defined number of substituents. This will apparently reduce the number of compounds unintentionally captured by the generic definition, estimated by industry at more than 40,000 substances, while retaining those that have not been found to cause harm. As the Minister said, the revised definition does not alter the position for class A drugs or the licensed medicines previously excluded.
When this order was discussed in the Commons, the Minister said,
“so that while those compounds that have been found to cause harm are captured by it, fewer compounds are unintentionally captured”.—[Official Report, Commons, 3/7/19; col. 1263.]
In view of the Commons Minister’s words, how many compounds will still be unintentionally captured by the amended order that we are discussing now, and what level of inconvenience or difficulty will that continue to cause the research community in the pharmaceutical and healthcare sector in respect of having to continue, where necessary, to apply for Schedule 1 licences? How cumbersome, time-consuming and time-delaying is the process of applying for Schedule 1 licences, the need for which this order is designed to reduce but apparently not eliminate, in respect of compounds “unintentionally captured” by the 2016 changes? Bearing in mind that the ACMD made its recommendation, which led to the Government making this draft order some 18 months ago, why has it taken as long as it has to reach this stage?