
Please follow us at @Synchrogenix where we offer a full complement of regulatory submission software & regulatory services.
Philadelphia, PA
Joined October 2009
- Tweets424
- Following179
- Followers267
- Likes7
GlobalSubmit retweeted
Speak with our submission strategy experts at #RSIDM18. We'll have giveaways & #RIM product demos. See how our latest software suite, including @GlobalSubmit MANAGE and COMMUNICATE can help your organization "manage" your submissions & "communicate" correspondence & commitments.
GlobalSubmit retweeted
Visiting our new eCTD software provider @GlobalSubmit at their booth here at #2016RAPS. We are excited to start working with them soon!
GlobalSubmit retweeted
#regis_ma MS Reg & clinical research alums Rob Labriola of @GlobalSubmit & Naveen Yamana of @Sunovion lectured on #eCTD on campus this week
GlobalSubmit retweeted
Excited that @GlobalSubmit Jason Rock will talk to @RAPSorg PHL mtg Dec 11. Registration opening soon
GlobalSubmit retweeted
Join Nov 5 @RAPSorg PHL chapt mtg to hear Jason Rock of @GlobalSubmit on global harmonization of eSubmissions ow.ly/CtsWT
GlobalSubmit retweeted
Learn more about modified risk tobacco products, filed applications & how to submit a public comment ow.ly/AZuq4 #TobaccoControl
GlobalSubmit retweeted
Electronic Submissions to CDER > FDA Clarifies Submission of periodic safety reports to the #eCTD
fda.gov/Drugs/DevelopmentApp…
GlobalSubmit retweeted
After Confusing Approval Process, #FDA Confirms Teva's Plan B One-Step Will get Exclusive Rights - #Regulatory Focus ow.ly/nfeO2
GlobalSubmit retweeted
FINALLY: FDA finalized upgrades to its validation tool - #eCTD Validation Criteria V2.1 in effect by April 30, 2013. ow.ly/ibuLG
GlobalSubmit retweeted
Quality one of FDA's 'Highest Priorities' in 2013, Agency Creating New #Quality Office - #Regulatory Focus ow.ly/i1Tx7 #FDA
GlobalSubmit retweeted
Here's the link to the Docket: Documents to Support Submission of an Electronic Common Technical Document; Availability ow.ly/hG3f6
GlobalSubmit retweeted
FDA’s December 2012 Guidance On IND And BA/BE Reporting – Part I ow.ly/hvolA
GlobalSubmit retweeted
Health Canada announces extension of deadline for using the old Canadian Module 1 DTD Version 1.0 to 30-Sep-2013 #eCTD ow.ly/hCFHP
GlobalSubmit retweeted
EMA developing a Central Repository for National Competent Authorities to search, browse and download CP #eCTDs ow.ly/htDgn
GlobalSubmit retweeted
Updates to FDA 356h and instructions #eCTD fda.gov/AboutFDA/ReportsManu…
GlobalSubmit retweeted
Australia to Launch Consultation on Development of eCTD Guidelines, Timetable > RAPS > News - Article View raps.org/focus-online/news/n…
GlobalSubmit retweeted
Slides from the webinar with Jason Rock of @GlobalSubmit are available on our blog: wp.me/p24Xam-NM. Thanks to Jason for a great talk!
GlobalSubmit retweeted
Still time to register for tomorrow's free webinar with @GlobalSubmit - Regulatory Electronic Submissions: #eCTD v4. wp.me/p24Xam-NM
GlobalSubmit retweeted
Register 4 next week's Free Webinar w/ @GlobalSubmit "Regulatory Electronic Submissions: #eCTD v4 Background & Drivers" wp.me/p24Xam-NM










