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.
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 is the first in a series that explores insights and approaches to attaining drug supply integrity while addressing the challenges of disconnected, opaque supply networks and Drug Supply Chain Security Act (DSCSA) regulatory compliance. Reserve Your Spot Today!
While virtualization is widely used in commercial enterprise environments, it has not to date played any significant role in High Performance Computing (HPC). During this webinar we discuss the promises and challenges in this new, emerging area. Reserve Your Spot Today!
Interest in using electronic patient reported outcomes (ePRO) on smart devices is on the rise. In this webinar, Emily Cantrell and Becky Baggett will share lessons learned working on a large phase 3 pain study that utilizes ePRO on tablet devices. Register Now!
This webinar will review regulatory guidance and practical strategies for designing viral clearance studies. These include appropriate scale-down of unit operations, virus spike-related considerations and validation (clearance evaluation) of manufacturing process steps. Reserve Your Spot Today!
This webinar will discus 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. 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.
Biopharma companies can never eliminate the risk of supply chain disruption, but they can prevent some problems and prepare themselves for others. Knowing every company in the supply chain--from tier one down--and having contingency plans in place are essential steps to foreseeing and responding to disruptions. Maps of supply chain risks give companies this knowledge. Register Now!
Join Pegasystems and Telerx to learn how the Pega platform is being utilized to support a multi-tenant client environment to engage patients during all phases of a product's life cycle, through a central touchpoint. Register Now!
Scientific workflows like light-sheet microscopy and next generation sequencing are pushing research groups to develop new methods to deal with such data-intensive instrumentation. Current, mostly serialized analysis pipelines can often take days to run and often there is no 'right analysis'. Reserve today to watch 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 to Watch Now!
Join this webinar to take part of the discussion evolving nature of metadata along with recent advancements and approaches developed by the IRODS Consortium and its members to capture, manage, and use meta-data to enable life science research workflows. Reserve today to watch 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 to Watch Now!
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 to watch now!
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!