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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This 3-part webinar series is specifically geared toward the non-science professional who needs to better understand industry terminology, science, techniques and issues. This series provides an overview of the science and technology used to enable discovery and the processes scientists use to discover new therapeutics. Download now.
Learn in this webinar how a comprehensive centralized chemicals Inventory system that is tightly integrated with other lab informatics systems – such as Electronic Lab Notebooks – reduces chemical management safety and compliance risks, allows laboratories to be more efficient, and reduces overall complexities and costs. Register Now!
The goals of translational R&D have placed a particular premium on the ability to rapidly collect, curate, and integrate information from a variety of sources. This presentation will discuss some of the challenges in building a sustainable technology infrastructure to support these activities, which will enable more sophisticated analytics and decision support. Reserve Your Spot Today!
Life sciences companies are now presented with huge amounts of data that incorporates real world evidence into the drug development and marketing efforts. The question now is whether this data is being used effectively, quickly, and whether it points to the right insights. This webinar offers real-world advice and specific pointers on using real world evidence data to best effect. Register today.
Regulators are becoming wary of self-assessments captured on paper, so join this session to learn what is currently driving ePRO decisions. Reserve Your Spot Today!
Learn in this webinar how a comprehensive centralized chemicals Inventory system that is tightly integrated with other lab informatics systems – such as Electronic Lab Notebooks – reduces chemical management safety and compliance risks, allows laboratories to be more efficient, and reduces overall complexities and costs. Register to Watch Now!
The next revolution in clinical trial execution is taking shape in the rapid adoption of mHealth technologies. PPD experts discuss how current PPD-conducted studies assess the feasibility of wearable data collection devices in trials to achieve focused endpoints and improve the patient experience. Register to Watch 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!
The FDA's Unique Device Identification (UDI) compliance date of September 24, 2016 for Class II device labelers is now less than one year away. Register today to learn why Class II UDI compliance is the biggest challenge yet, 5 steps to a timely submission, and more.
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 to Watch Now!
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 to Watch Now!
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!
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!
In this webinar, Dr. Frank Smith will explore advances in precision medicine and how it is affecting clinical research. As a pediatric hematologist/oncologist, he will use his extensive clinical and research background as a backdrop for the discussion. Register to Watch Now!
Join us for a deep dive into the pricing challenges and the best-practices you can follow to not only survive the new cost-out/value-in ecosystem trying to disrupt the Med Tech industry, but actually exploit these changes to establish competitive advantage. 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!