Dublin, June 20, 2023 (GLOBE NEWSWIRE) -- The "Regulatory report: Labelling requirements for medical cannabis products - EU and UK" report has been added to ResearchAndMarkets.com's offering.
This report seeks to outline the labeling and packaging requirements that cannabis-containing medicinal products need to comply with when their placing on the European market is authorized.
The European regulatory framework for medicinal products covers authorized cannabis-containing pharmaceutical products. The latter are subject to the general requirements applicable to medicinal products, meaning that the European Union does not have a specific framework for cannabis-derived medicinal products.
This regulatory report will provide you with:
- A clear and detailed understanding of current regulatory requirements affecting this sector in a specific jurisdiction, enables you to be confident your business and your products are compliant.
- The ability to plan ahead for specific regulatory changes.
- Strategic understanding of the jurisdiction's policy climate enables you to forecast how it might affect business development.
- Sources of further information, for example, links to full texts of legislation and contact details for relevant government offices.
Key Topics Covered:
- Executive summary
- Introduction
- Overview of the authorisation procedure
- Common labelling requirements
- Outer packaging
- Immediate packaging
- Package leaflet
- Labelling requirements for medicinal products in the UK
- Labelling guidelines for marketing authorization holders
For more information about this report visit https://www.researchandmarkets.com/r/80uxjg
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