Cannabis

All questions on this topic
What is being done to prevent abuse in connection with the lifting of the ban on cannabis for medical purposes?
Why I am obliged to enter the data in a reporting system?
Are there any restrictions on formulations or dosage forms?
What has changed for physicians?
What data has to be entered in the reporting system?
For what indications are medicinal cannabis products mainly used?
Do I still need a licence to conduct medical research involving cannabis?
What products are available for treatment?
In what cases is an exceptional licence from the FOPH still required?
Who prescribes medicinal cannabis products?
As regards medicinal cannabis products, what has changed with the revision of the Act?
What happens to the data which is collected?
Why was a revision of the Act needed?
Is data protection assured in connection with mandatory reporting by my physician?
How will the effects of the revised Act be monitored in Switzerland?
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