Combination Drug Products: A Development Roadmap to Clinical Trials

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.