Zdrowie i gospodarka · 14.06.2002
International Conference on Harmonisation; Draft Guidance on Electronic Common Technical Document Specification; Availability
The Food and Drug Administration (FDA) is announcing the availability of a second draft guidance entitled "Electronic Common Technical Document Specification" (eCTD). The draft guidance was prepared under the auspices of the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH). The draft guidance defines the means for industry-to-agency transfer of regulatory information that will facilitate the creation, review, life cycle management, and archiving of the electronic submission. The draft guidance is intended to assist industry in transferring electronically their marketing applications for human drug and biological products to a regulatory authority.