Welcome to the Library, where you'll find a selection of industry resources including eBooks, Whitepapers, Webinars, Survey Reports, Research Reports and more.
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For the biopharma industry in particular, regulatory compliance is a huge issue. In this webinar, we will discuss how an effective Content Management program can provide a framework to aid biopharma companies in compliance. Register Today!
Clinical trial enrolment continues to be a challenge for the pharmaceutical industry. We will look at how utilizing a Functional Service Model can allow you access to experts that can develop, execute, and analyze your recruitment (and retention) strategies to achieve enrolment success. Register Now!
FDA's Breakthrough Therapy, Accelerated Approval, Priority Review, and Fast Track may speed product approval. In this webinar, David Shoemaker will explain the differences, describe strategies to determine which program may be right for you, and discuss FDA requirements for each. Register Now!
Attend this webcast for an interactive panel discussion around the findings of a blinded industry survey on eSource in clinical trials – including current and anticipated growth, capabilities critical to eSource, and expected vs. actual benefits. Reserve Your Spot Today!
This webinar will discuss how the emergence of the ability to share documents and data across thousands of miles instantly has pulled biopharma companies in two opposing directions. Companies want, even need, the interconnectivity that is facilitated by the Internet, but feel equally strongly about controlling who can view and interact with their data. Watch it now!
This webinar will feature experts in drug development, regulatory processes and managed care who can shed light on the impact of escalating drug prices and provide tips on navigating these challenges. Register to Watch Now!
With biopharma companies hitching their long-term growth plans to success in emerging markets, they can ill-afford for logistical difficulties in new territories to scuttle their ambitions. This is a real risk, though. Transporting drugs to patients in Brazil, India and China is fraught with multiple challenges for which experience of shipping products in the West offers scant preparation. Register to Watch Now!
Pharma companies can employ several strategies for obtaining expedited approvals-including, in some cases, acquiring them from other companies. This webinar will feature regulatory experts from the pharma industry who can provide tips on navigating these programs. Register to watch now!
With the relentless drive to reduce costs and increase innovation, B2B collaboration is increasingly becoming the mainstay of research and development (R&D). From pharmaceuticals to energy, healthcare to consumer goods, IDBS helps R&D teams make discoveries that have the potential to transform the lives of populations worldwide. Reserve Your Spot Today!