Please follow us at @Synchrogenix where we offer a full complement of regulatory submission software & regulatory services.
Philadelphia, PA
Joined October 2009
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The GlobalSubmit team is alive and well with @Synchrogenix, the strategic regulatory & scientific consultancy that acquired us last year. Please be sure to follow us at @Synchrogenix for news, upcoming webinars & events, and industry updates.
We can help with submission outsourcing. globalsubmit.com/education/b… teapawt.net/Synchrogenix/status/96…
It's 2018, yet some paper applications are still alive & well. However, their days are numbered. The May 5 @US_FDA #eCTD mandate is upon us. Is your company prepared to implement the FDA’s regulations for eCTD submissions of INDs, NDAs & DMFs? Read more: wp.me/p9rwl0-3cw
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.
We're so proud of this! You won't want to miss tomorrow's #RIM #webinar. teapawt.net/Synchrogenix/status/95…
The release of @GlobalSubmit RIM marks a great achievement for our organization! Register for the Jan. 31 #Regulatory Information Management #RIM product demo today: tinyurl.com/ycaydowb
If you haven't converted to #eCTD format yet, sign up for this webinar today! teapawt.net/Synchrogenix/status/95…
Are you prepared to implement the #FDA's regulations for #eCTD submissions of IND/NDA? Register for our webinar to learn about our publishing services & how we can help you achieve submission success simply, quickly, & cost-effectively. tinyurl.com/y73g7cga
GlobalSubmit is launching a pair of #Regulatory Information Management products. Catch the demo tomorrow at 2 p.m...bit.ly/2kimOuN
GlobalSubmit is excited to announce the launch of a pair of RIM products - COMMUNICATE and MANAGE bit.ly/GSRIM
FDA is planning to add new #eCTD validation errors (2 high, 2 med) related to submission of study data...bit.ly/2eNSVCB
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 Product Manager Rob Connelly is part of the eCTD FDA Module 1 panel at #RAPS2016 this afternoon. bit.ly/2crF8iu
Stop by booth 529 to check out GlobalSubmit's new solutions for document management and regulatory information management #RAPS2016
Chief Technical Officer Jason Rock writes that FDA's New M1 is a bridge to #eCTD v4...bit.ly/2cMrXbx
Join GlobalSubmit in #RTP on 9/22 as we discuss Regulatory Publishing Best Practices for eCTD submissions...conta.cc/2cBKOoO
GlobalSubmit 2016 v(10.0) is compliant with the latest regional specs for Australia, EU, and Switzerland...bit.ly/2bwMOBb #eCTD
The original Project Lead for Regulated Product Submissions, Jason Rock, explains the key points of #eCTD v4...bit.ly/2by5kpN
Stop by Booth 2052 to hear more about GlobalSubmit's solutions for life sciences document management and RIMS #DIA2016
As of 5/31/2016, CDER will issue a 3rd ESG acknowledgement for NDA, ANDA, BLA, IND or DMF when submissions complete validation & processing
The FDA's eCTD mandate for certain application types is 365 days away. @Evan_R says the time to prepare is now...bit.ly/1WaiYT5
GlobalSubmit retweeted
#regis_ma MS Reg & clinical research alums Rob Labriola of @GlobalSubmit & Naveen Yamana of @Sunovion lectured on #eCTD on campus this week