A Q&A guide to the commercialisation of healthcare in Poland.

This Q&A provides an overview of the regulatory framework for the commercialisation of medical products in Poland. It covers the key requirements for manufacturing, advertising and selling drugs, medical devices, biological products and natural health products.

To compare answers across multiple jurisdictions, visit the commercialisation of healthcare Country Q&A tool.

Full content of the article is available at: https://uk.practicallaw.thomsonreuters.com/5-618-2077?__lrTS=20171005153710030&transitionType=Default&contextData=(sc.Default)  

Source: Practical Law Global Guides - Thomson Reuters, 2016