Mondaq-Dentons(UK)European Union: Will Medical Cannabis Soon Be Part Of The European Single Market?
Prior to discussing the recent legal developments in the field of medical cannabis, it is important to distinguish between medical cannabis and EU-approved medicinal products derived from cannabis. Medical cannabis is cannabis grown for medical purposes, whereas EU-approved medicinal products encompass certain medicines derived from cannabis and containing an amount of the active ingredients of cannabis, such as tetrahydrocannabinol (THC) and cannabidiol (CBD). The EU has approved some medicinal products derived from cannabis but has not yet approved medical cannabis itself as a medicinal product.
On February 13, 2019, the European Parliament adopted a resolution on the use of cannabis for medicinal purposes (2018/2775(RSP)), after evidence had been provided on the medicinal power of cannabis, i.e. cannabis or cannabinoids that can help to increase appetite and decrease weight loss associated with HIV or AIDS and alleviate symptoms of epilepsy, asthma, cancer and Alzheimer’s.
In this resolution, the European Commission and the member states are urged to work on the legal framework of, and the research into, the use of cannabis for medicinal purposes. However, and contrary to the US and Canada, no EU-wide policy for medical cannabis has been enacted yet.
In the EU each member state is competent to decide whether the cultivation and use of medical cannabis is legal, and is responsible for regulation. Consequently, the legality and regulation of medical cannabis varies widely among the member states.
Medical cannabis can be defined as the cannabis distributed by a pharmacy, intended for therapeutic purposes and consisting of a number of different active ingredients such as a combination of tetrahydrocannabinol (THC) and cannabidiol (CBD).
Five months after the parliament’s resolution, on July 17, 2019, the European Commission clarified the difference between medicinal products derived from cannabis and medical cannabis (SP(2019)327).
Only medicinal products fall within the scope of the pharmaceutical legislation of the EU and only these products can be placed on the market after a marketing authorization has been granted by the competent authority of a member state or by the European Commission1. Until now, only a few medicinal products derived from cannabis have received market authorization in the European Union, such as Epidiolex (by the European Commission) and Sativex (in some member states).
As for medical cannabis, no marketing authorization can be granted in the EU since cannabis as such has not yet been approved as a medicinal product by the European institutions. Therefore, it is up to the member states to determine whether or not it is authorized to grow and use medical cannabis on their territory.
The legalization of cultivation and use of medical cannabis in the EU
As early as 1961, the United Nation’s Single Convention on narcotic drugs allowed the cultivation of cannabis insofar as one or more national agencies have been established which have the exclusive right to import and export cannabis and are responsible for wholesale trading and the maintenance of the cannabis stocks. The competent agencies would furthermore have the exclusive right to grant licenses to companies to grow cannabis. However, the agencies will be solely responsible for the purchase of the entire cultivation of cannabis and are subsequently in charge of the sale of cannabis to pharmacies, hospitals and research institutes such as universities.
Over the years, several member states have set up such an agency, opening the path for the decriminalization/legalization of the cultivation and use of cannabis, however, for medical purposes only.
In 2017, the Federal Institute for Drugs and Medical Devices (BfArM) established the Cannabis Agency in Germany. The agency has granted the first licenses to German companies, but also to Aurora Cannabis Inc., a listed Canadian company, making Germany the cannabis market leader in the EU.
Many European countries have followed suit, such as the Netherlands with the Office of Medicinal Cannabis (BMC), Spain with the Agency for Medicines and Health Products (AEMPS) and Portugal with an agency called Infarmed. The Belgian cannabis agency (Cannabisbureau) has not yet become operational. A law for the creation of the Belgian cannabis agency was enacted in April 2019, but the Royal Decree, laying down detailed rules about the function and operations of the agency, is still pending.
Policy confusion within the EU
The different approaches on the legality of cultivation and use of (medical) cannabis in the member states have led to a policy paradox within the European Union, causing complications for patients in several member states. For example, a patient that has obtained a prescription for medical cannabis in Belgium has to cross the border and rely on a Dutch or German pharmacist to receive the medical cannabis. From the moment he/she crosses the border to Belgium again, he/she can be penalized since the cultivation and use of cannabis is a criminal offence in accordance with Belgian law.
To avoid these complications, all member states should create a cannabis agency in accordance with the UN Single Convention of 1961 on narcotic drugs and harmonize the regulation(s) on the cultivation and use of medical cannabis. EU legislative acts, such as directives, can help member states harmonize their regulation(s) on medical cannabis and can enable medical cannabis to become part of the European Single Market in a harmonized and transparent manner. So far, the EU does not seem to be in any hurry to provide guidance on this confusion.
If you are interested to learn more about the legislation concerning cannabis in the European Union or have any questions, do not hesitate to contact the Brussels office of Dentons Europe LLP. Our professionals are available to provide any tailor-made advice at short notice.
Such as Directive 2001/83/EC of the European Parliament and of the Council of November 6, 2001, on the Community code relating to medicinal products for human use and Regulation (EC) 726/2004 of the European Parliament and of the Council of March 31, 2004, laying down Community procedures for the authorization and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency.
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