This seminar will examine the routes available for obtaining scientific advice in Europe (including covering the recent changes to the CPMP and MHRA procedures), as well as in the US and Japan, and will explore the means of securing the best possible input and integrating advice from several different sources into a single global development programme.
Event Website : SCIENTIFIC ADVICE - Optimising Regulatory Input Into Drug Development

Location:	Hotel to be advised, London
Contact:	Leigh White leigh@management-forum.co.uk 44 1483 730071
Organization:	Management Forum Ltd
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