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Event Details


IP for Pharmaceutical Regulatory Affairs

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Who should attend?

This seminar will be of interest to development and regulatory managers working in the pharmaceutical industry. It will also be relevant to anyone requiring an overview of the key IP issues relating to regulatory affairs.


Course overview


This practical one day course will provide an overview of Intellectual Property (IP) for those working in Regulatory Affairs.

IP is a fundamental contributing factor to the overall regulatory strategic approach that a company may take and recognition of the different aspects of IP and in uences is essential in modern regulatory affairs. Attendance will enable you to understand IP aspects and their impact and in uence on regulatory strategy. Key issues covered will include patents, trademarks and copyright as well as Data and Market Exclusivity for global pharmaceutical products. The course will also discuss the EU and FDA regulatory process, highlighting one of the fundamental differences between EU and US systems and the link to patents.


Leigh White

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