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Combination Drug Products: A Development Roadmap to Clinical Trials

 
  June 24, 2021  
     
 
Xtalks, Online
2021-07-13


In this webinar, the speakers will examine what you need to know about your product to effectively support these transitions, including understanding the target product profile, critical quality attributes, product and device variability, analytical testing, regulatory requirements and the interaction of testing and manufacturing parameters. Similarly, the receipt, inspection, and assembly of the device components will be discussed within the context of their impact on device efficiency, and thereby their effect on product delivery and performance. Aspects of device evaluation will also be discussed in terms of performance and more routine testing such as assays.
 
 
Organized by: Xtalks
Invited Speakers:

Justin Lacombe, PhD, Chief Scientific Officer, Experic LLC

 

Julie D. Suman, RPh, PhD, President, Scientific Affairs, Next Breath

 

 
Deadline for Abstracts: -
 
Registration: Register for this webinar to learn about critical steps to transfer the development process, sponsor and service provider responsibilities, and an efficient framework to collaborate with partners will be presented to help minimize delays and accelerate timelines on your pathway to the clinic.
 
   
 
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