Cannabis

All questions on this topic
Are there any regulations concerning the production of medicinal cannabis products?
Why was a revision of the Act needed?
As a prescriber, am I also required to enter patient data on treatments already in progress?
What is the procedure and where do I have to submit reports on treatment?
Is data protection assured in connection with mandatory reporting by my physician?
What has changed for physicians?
What is being done to prevent abuse in connection with the lifting of the ban on cannabis for medical purposes?
What has changed for pharmacies?
As regards medicinal cannabis products, what has changed with the revision of the Act?
How much does a medicinal cannabis product cost? What are the estimated monthly costs of treatment?
What data has to be entered in the reporting system?
What duties have to be fulfilled by physicians prescribing medicinal cannabis products?
Are there any restrictions on formulations or dosage forms?
For what indications are medicinal cannabis products mainly used?
Do I still need a licence to conduct medical research involving cannabis?
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