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The course, a Thomson Reuters Cortellis Regulatory Online Learning module, discusses the establishment of the International Conference on Harmonisation (ICH) technical requirements for registration of pharmaceuticals for human use by the EU, Japan, and United States. ICH membership, structure, and milestones are explored. The course describes the process for harmonisation, implementation of guidelines, and achievements reached in the three regions. The course concludes by describing the impact of ICH global harmonisation efforts on non-ICH countries.
Professionals and experts in the pharmaceutical, biotechnology, and medical device fields
Participants who complete this course should be able to:
The course takes an average of one hour to complete.
Linda Belmont, DIAPhone +1.215.293.5818Linda.Belmont@diahome.org
Click here for minimum system requirements.
Unless otherwise disclosed, the statements made by speakers represent their own opinions and not necessarily those of the organization they represent, or that of the Drug Information Association. Speakers, agenda and CE information are subject to change without notice. Recording of any DIA educational material in any type of media is prohibited without prior written consent from DIA.