Mastering Regulatory and Development Strategies for Generics

Gain a strategic insight into requirements for developing generics from a global perspective and an overview of the generics market.

27-28 May 2014 at Radisson Blu Edwardian Grafton Hotel, United Kingdom

Education & Learning, Pharmaceuticals/Drug Discovery

Mastering Regulatory and Development Strategies for Generics 27-28 May 2014 Radisson Blu Edwardian Grafton Hotel, United Kingdom
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The majority of all pharmaceutical company revenues now face generic competition. This represents an unprecedented growth in the generics market. With more and more patents expiring since 2006, this global expansion looks set to continue.

Bringing a generic drug to market can be fraught with regulatory challenges and compliance issues. This course will allow the participants to:

• Create effective regulatory affairs strategies for post-patent expiry
• Understand EU and US generic requirements
• Maximise generic market-share potential
• Devise best strategy for approval in the EU and US

Price: Book before the 29th April 2014: £1,395.00 + (VAT @ 20.00%) = £1,674.00, Book after the 29th April 2014: £1,495.00 + (VAT @ 20.00%) = £1,794.00

When
From: May 27, 2014 09:00
To: May 28, 2014 17:00
Where

Radisson Blu Edwardian Grafton Hotel, 130 Tottenham Court Rd, W1T 5AY, United Kingdom

Category

Education & Learning, Pharmaceuticals/Drug Discovery

Contact email
rachael.ouston@informa.com

External link

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