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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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April 08, 2011 |
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Radisson Blu Hotel , Tallin, Estonia
Jul 4 2011 7:00AM - Jul 6 2011 4:00PM
This 3-day workshop will highlight the benefits of the ICH (1) Common Technical Document (CTD) for manufacturers and regulators. Harmonisation of regulatory requirements and high quality of a registration dossier facilitate the registration procedure and are essential for both generics as well as innovative medicines. A comprehensive description of the CTD structure will be provided by an expert faculty from regulatory agencies and industry. The workshop will focus on the specific regional EU (European Union) requirements taking into account the recent ICH-Q guidelines.
An additional 2-day programme will be provided by the WHO for regulators from 7-8 July.
Presentations will be given in English. Simultaneous translation into Russian will also be provided.
(1) International Conference on Harmonisation of Technical Requirements for Registration of
Pharmaceuticals for Human Use (www.ich.org) Event Code:
11580
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Organized by:
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DIA Europe |
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Invited Speakers:
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See website for speaker information
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Deadline for Abstracts:
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Call contact
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Registration:
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The DIA Europe Customer Services Team will be pleased to assist you with your registration. Please call us on +41 61 225 51 51 from Monday to Friday between 08:00 and 17:00 CET Email diaeurope@diaeurope.org
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E-mail:
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diaeurope@diaeurope.org
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