This seminar presents all the requirements to obtain FDA permission to market a Drug product in the USA. To find out the fastest and most cost-efficient way onto the USA marketplace this seminar is a must. This seminar introduces FDA and its laws, regulations, policies and guidelines. Starting with Drug development this seminar continues with discussions on the testing requirements for new chemical entities (NCE) and the IND system which leads to Drug clinical testing.

Date : 4th December 2014 to 5th December 2014

Place : United States, Hong kong

Website :http://www.globalcompliancepanel.com/seminar#page=2

Contact Person:Event Manager

Description:

This seminar presents all the requirements to obtain FDA permission to market a Drug product in the USA. To find out the fastest and most cost-efficient way onto the USA marketplace this seminar is a must. This seminar introduces FDA and its laws, regulations, policies and guidelines. Starting with Drug development this seminar continues with discussions on the testing requirements for new chemical entities (NCE) and the IND system which leads to Drug clinical testing.

This seminar presents all the requirements to obtain FDA permission to market a Drug product in the USA. To find out the fastest and most cost-efficient way onto the USA marketplace this seminar is a must. This seminar introduces FDA and its laws, regulations, policies and guidelines. Starting with Drug development this seminar continues with discussions on the testing requirements for new chemical entities (NCE) and the IND system which leads to Drug clinical testing. will be held in Hong kong,United States on date 2014-12-05

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Deadline for abstracts/proposals : 2nd December 2014

Keynote Speakers :

Check the event website for more details.