Contact
Good Products Give Podcast on understanding eCTD
Following a general move by the pharmaceutical industry toward electronic-based processes, both the FDA and its European counterparts are now recommending the use of the Electronic Common Technical Document (eCTD) for regulatory submissions of pharmaceutical products in the USA , Europe and Japan . This podcast discusses the challenges faced by companies operating in the pharmaceutical sector, and looks at eCTD – what it is, when it’s used and how submission can be facilitated, as well as implications for laboratory informatics.
Listen to the Podcast here >
With thanks to our partners ISI.