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.
Regulatory authority meetings require strategic preparation to ensure a successful outcome. In this webinar, Lauren Neighbours, Clinical Research Scientist, and Dana Minnick, Regulatory Scientist, discuss how to approach FDA meetings to get the most benefit for your development program. Register Now!
Lessons-learned from Executing Complex Medical Device Trials - Special focus on Cardiovascular Device
Medpace uses its vast experience in CV trials as a backdrop to discuss the critical factors for designing and executing studies for complex and high-risk medical devices. Register Now!
This webinar will explore capsules' utility in a range of applications, including bioavailability enhancement, modified release, pediatric solutions, & fixed dose combinations. Learn more about how capsules enable rapid advancement of products built on QbD principles and supported by PAT. Register today!
This webinar will address the impact of medication non-adherence in clinical trials. Accurate adherence measurement is necessary to evaluate a compound's true potential and increase the likelihood of a successful trial outcome. Register today!
BBK Worldwide hosts a webinar exploring this new connected health model and its impact on clinical research. Join their expert panel, which includes mHealth experts from BBK Worldwide, Oracle and Empatica, and learn key strategies for successful implementation. Registration is free – click here.
This webinar will summarize the core scientific concepts needed to develop a global observational study protocol that describes or evaluates a therapeutic treatment in patients under conditions of usual care, in terms of clinical, humanistic and economic outcomes for a variety of key stakeholders. Register Today!
This webinar will demonstrate how government contracts differ in the marketplace. Business cases from the HHS - Biomedical Advanced Research and Development Authority and the DOD will provide a thorough understanding to navigate this landscape of management, legality, contracts, and oversight. Reserve Your Spot Today!
Hear how Kythera Biopharmaceuticals reduced their TMF reconciliation time by 40% with their TMF strategy. Sign up for the webinar here.
At first glance, the TMF reference model seems daunting, especially for smaller companies. In this webinar, Kristen Snipes and Missy Lavinder share tips and tricks for making the process manageable based on their own recent experience implementing the model. Register to Watch Now!
Learn how Natera leverages cloud-based content management systems to simplify collection, management, and secure access of controlled documents - improving operational efficiency, and enabling agility amidst increasing procedural requirements. Register to watch now!
Here we describe discovery approaches designed to broadly survey the skin metabolome as well as focused metabolomic assessment of sebum, stratum corneum, skin biopsy, cell culture and reconstructed skin models across a variety of conditions. Further, we share results from recent publications and practical clinical case studies. Register to Watch Now!
In December 2014, FDA released the Guidance for Industry "Providing Regulatory Submissions in Electronic Format—Standardized Study Data." This webinar will review the guidance and discuss the implications for Sponsors currently conducting studies and for those starting new studies soon. Register to Watch Now!
Join our lively discussion of the five most innovative M&A and Licensing deals from 2014, selected as nominees for the Breakthrough Alliance Award 2014. Thomson Reuters Recap analysts have examined hundreds of biopharma deals negotiated in 2014 and used both subjective and objective criteria to identify the top five contenders in each category. Register to watch now!
This webinar will bring together pharmaceutical executives across a range of functions—from marketing to regulatory affairs to development—to discuss these trends and suggest strategies for thriving in this increasingly vigilant environment. Register to Watch Now!