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PROMOTIONAL TOOLKIT

2019 PDA/FDA Joint Regulatory Conference

 

Join the Conversation

Stay engaged and informed on the 2019 PDA/FDA Joint Regulatory Conference by following PDA on social media @PDAOnline and on our LinkedIn page. Be sure to follow the event hashtag: #2019PDAFDA

 

Spread the Word

At the 2019 PDA/FDA Joint Regulatory Conference, you'll join nearly 1,000 of your peers, regulators, and industry experts to discuss how innovations in manufacturing are impacting quality, compliance, and regulatory paradigms and advancing the continued supply of novel drugs, biologics, and combination products. Help us get the word out and promote your attendance at this year's event.

2019 PDA/FDA Joint Regulatory Conference

 

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Check out the below resources for you to share with your network to promote your involvement in the 2019 PDA/FDA Joint Regulatory Conference!

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Request a Press Pass

Do you work for the press? Press passes are available to bona fide members of the press. Request a press pass today!


Let's get social

Sample Posts
Twitter
  • Looking forward to hearing FDA’s Dr. Peter Marks and Dr. Marschall S. Runge headline an esteemed lineup of speakers discussing how innovation is being used to address the continued supply of high-quality medical products to patients. #2019PDAFDA http://bit.ly/32SVbhJ
  • #2019PDAFDA is the best place to engage with senior U.S. FDA officials and industry leaders regarding the most pressing manufacturing, quality, supply, and compliance issues facing the industry. Join me at the Conference to find out why!
  • There is no better forum for engaging with senior officials from the U.S. FDA and industry leaders than #2019PDDAFDA. Join me to explore the latest advances in innovation & technology, quality & compliance, lifecycle implementation, and inspections & audits during this informative Conference! http://bit.ly/32SVdWT
LinkedIn
  • I am looking forward to hearing Peter Marks, MD, PhD, Director, CBER, U.S. FDA, and Marschall S. Runge, EVP, Medical Affairs, University of Michigan, keynote the 2019 PDA/FDA Joint Regulatory Conference. I hope you will join us and other industry leaders to get the latest insights on how you can improve the continued supply of high-quality drugs, biologics, and novel combination products to patients. Informative plenary, concurrent, breakfast, and interest group sessions will address the most important pharmaceutical manufacturing issues in the medical products regulatory landscape. I’ve got the new Lunch with the Regulators session on my agenda – I encourage you to be there as well! http://bit.ly/32Sa3wO
  • I am attending the 2019 PDA/FDA Joint Regulatory Conference – are you? Please join me to as we hear from industry and regulatory leaders on the latest manufacturing innovations, learning from failures to implement sustainable CAPAs, and the evolving regulatory landscape. Senior officials from the U.S. FDA will present the always-popular Center and Compliance updates. I plan to attend the new Lunch with the Regulators session where attendees will get answers to their regulatory and compliance questions in a roundtable format. I hope to see you there! http://bit.ly/32Uhxze
  • Sept. 16-18, I will be taking advantage of unparalleled opportunities to engage with global industry and regulatory experts at the 2019 PDA/FDA Joint Regulatory Conference. The distinguished lineup of speakers will present on the latest news on ICH Q13, cGMP challenges associated with cell and gene therapies, inspections and audits, and much more. I am also looking forward to the multiple opportunities to connect with peers and experts during the Interest Group sessions and Lunch with the Regulators. If you want the be part of the premier pharmaceutical quality conference, be sure to join me! http://bit.ly/32UhrYo