Top Tweets for #pdafda
How are biopharma companies managing raw material risk in advanced therapies? @FDA, @genentech, and @MinarisRM discuss material qualification, supplier oversight, risk-based testing, and GMP expectations. Read more: https://t.co/csYvFF1C4X
#CellGeneTherapy #PDAFDA #GMP

Eagle team had a great time at the #PDAFDA. We appreciated the informative sessions, meaningful conversations, and shared focus on people, science, and regulation. Thank you to everyone who stopped by our booth and congratulations to our raffle prize winner.
#eagleanalytical

#PDAFDA Joint Regulatory Conference is underway, and the Eagle Analytical team is on site and ready to discuss the analytical, microbiological, and compliance solutions that help support quality and patient safety. Stop by our tabletop is #322.
#eagleanalytical #consulteagle


A special thank you to our #PDAFDA Silver Supporter, @LachmanConsult! Be sure to make time to visit them in the Exhibit Area.

Thanks to our #PDAFDA Silver Supporter, Sparta Systems, a @Honeywell Company! Be sure to stop by their tabletop while visiting the Exhibit Area.

The discussion continues at #PDAFDA with presentations by Machelle Eppler and Michelle P. Logan, both from @thermofisher, followed by a Q&A!
#PDAFDA is underway! @FDACDERDirector Dr. Patrizia Cavazzoni is launching the 32nd #PDAFDA by discussing maintaining quality assurance of medicines through sustainable compliance.
#PDAFDA is next week in DC! If you'll be there, make sure to stop by our booth to say hi, and be sure to catch our CEO's talk on the future of regulatory intelligence.

See you in DC! With more than 40 FDA experts participating as speakers and panelists, #PDAFDA is the place to be 18-20 Sept. for the latest on important issues related to CGMP and quality assurance. Livestream option also available! https://t.co/4yQsyfVw0B

π We are very much looking forward to this year's #PDAFDA in Washington, DC, hosted by the fantastic team at @pdaonline. Always great to reconnect with old friends and make new ones. If you'll be there, let us know! Our CEO will be presenting on the future of #regulatoryintelligence

Donβt miss #PDAFDA, the only pharmaceutical CGMP conference cosponsored by both the FDA and industry. Key to this conference are case studies providing expert insight and effective practices to ensure quality for the patient. Register by 23 July to save.
https://t.co/N3NOYC2sea

With 6 plenary sessions, 15 concurrent sessions, 9 interest group sessions, 8 breakfast sessions, and countless opportunities for interacting with regulatory and industry representatives, #PDAFDA is the place to be for expert insights!
https://t.co/NQ2DHgBnSz
If youβre looking for insights into ensuring consistent good manufacturing practices that assure drug quality, then register now for #PDAFDA! The agenda includes crowd favorites such as Center and Compliance Office Updates, and Lunch with the Regulators! https://t.co/wFgNQy9AO1

Take advantage of an unrivaled forum for open discussion between FDA and industry CGMP experts on current issues relating to manufacturing and quality assurance at #PDAFDA, 18-20 Sept. in Washington, DC. Save big β register by 23 July!
https://t.co/PaWCg2dgEZ

Plan now for #PDAFDA, the only joint FDA-industry co-sponsored pharmaceutical CGMP conference, 18-20 Sept. in Washington, DC, for expert insights on current issues relating to manufacturing and quality assurance. Early registration savings end 23 July! https://t.co/cXH6CErEgq

It has been two months since #PDAFDA! See what Early Career Professionals had to say about attending this conference while participating in our Mentorship Program.
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