Harv Martens retweeted
Revision of EU eCTD Module 1 Specification - Due to accession of Croatia: lnkd.in/xhWdMK
Harv Martens retweeted
In Shift, FDA to Require eCTD for all NDA, ANDA, BLA and IND Submissions | RAPS regualtory focus raps.org/focus-online/news/n…
Harv Martens retweeted
Australia to Launch Consultation on Development of eCTD Guidelines, Timetable > RAPS > News - Article View raps.org/focus-online/news/n…
Harv Martens retweeted
Australian TGA re-issues RFT for software tool to assist TGA's regulatory review/management of eSubs #ectd tenders.gov.au/?event=public…
Harv Martens retweeted
The long-awaited update from EMA on XEMVPD specification, requirements, vocabularies is out bit.ly/yH7jfY
Harv Martens retweeted
European Medicines Agency - European Medicines Agency launches electronic application form pilot ema.europa.eu/ema/index.jsp?…
Harv Martens retweeted
new from Antoinette Azevedo Good/Bad Authoring Practices and the Impact on #eCTD Quality and Compliance box.com/s/33eat7v001nud46csi…