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?
What has changed for physicians?
What has changed for pharmacies?
What data has to be entered in the reporting system?
Where can I obtain further information on the reporting system?
Where can I obtain support if I have queries on system data entry?
What is the procedure if treatment is discontinued by a patient?
Which medicinal cannabis products are affected by the revision of the Act?
What prescriptions have to be recorded in the reporting system?
As a physician providing treatment, how do I benefit from the data collection programme?
Why I am obliged to enter the data in a reporting system?
For how long do I have to submit reports on each individual treatment?
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