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Pharma & Medical Device Regulation

Published: December 2019

In 18 jurisdictions worldwide



Pharma & Medical Device Regulation provides a timely and comprehensive overview of the latest legislative and regulatory develops affecting this rapidly changing industry. Topics covered include: health services framework and competent authorities; clinical practice; marketing authorisation; amending authorisations; recall’ promotion; enforcement of advertising rules; pricing and reimbursement; off-label use and unlicensed products and sale and supply.  

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