ESCHBORN, Germany--(BUSINESS WIRE)--Image Solutions, Inc. (ISI), a leading provider of software and services to streamline the drug development and regulatory approval process, today announced that ...
In 2005, the heads of the European medicines agencies agreed that all EU member states must have the infrastructure and processes in place to handle only electronic Common Technical Document (eCTD) ...
PHILADELPHIA, Dec. 18, 2012 /PRNewswire/ --LORENZ Life Sciences Group launched today their groundbreaking new offering in the US market - docuBridge ONE, the eCTD Workstation Solution. docuBridge ONE ...
Rapidly growing research foundation replaced existing eCTD solution with PhlexSubmission to improve the speed, quality, and cost-effectiveness of submission process "We launched the Foundation this ...
This course will offer insight into the compilation of the eCTD, share experience and best practice gained during eCTD submissions in the EU, and the eCTD review process. The focus will be on ...
DUBLIN--(BUSINESS WIRE)--The "eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada" webinar has been added to ResearchAndMarkets.com's offering. This four day webinar series (each day 3 ...
Regulators at Health Canada have announced the finalization of guidance intended to assist sponsors in preparing electronic common technical documents (eCTDs) to submit their pharmaceutical dossiers ...
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