The Library

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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FDA's Expedited Development and Approval Programs

Webinar | Tuesday, October 20th | 1:00pm ET / 10:00am PT | Presented by: Rho

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!

eSource in Clinical Trials: Where Are We Today, and Where Next?

Webinar | Wednesday, November 4th | 11:00AM ET / 8:00AM PT | Presented By: Oracle

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!

mHealth, the Next Revolution in Clinical Trials

Webinar | Tuesday, November 10th | 11am ET / 8am PT | Presented by: PPD

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 Now!

Addressing Patient Recruitment Challenges through a Flexible Sourcing Model


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!

The Changing Landscape of Enterprise Content Management

Webinar | NOW AVAILABLE ON-DEMAND | Presented By: Collaborative Consulting

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!

How to enable anywhere, any data access without compromising security

Webinar | NOW AVAILABLE ON-DEMAND | Sponsored by: M-Files

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!

Navigating Escalating Drug Prices and the Need for Affordable Alternatives

Webinar | NOW AVAILABLE ON-DEMAND | Sponsored by: Elsevier

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!

Precision Medicine: Opportunities and Challenges for Clinical Trials

Webinar | NOW AVAILABLE ON-DEMAND | Presented by: Medpace

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!

Getting MedTech Pricing Right in the Evolving Healthcare Ecosystem

Webinar | NOW AVAILABLE ON-DEMAND | Presented by: Model N

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!

How to Prepare Your Supply Chain for Emerging Markets' Novel Challenges

Webinar | NOW AVAILABLE ON-DEMAND | Sponsored by: UPS

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!

Taking Advantage of New FDA Programs for Expediting Drug Development

Webinar | Now Available On Demand | Sponsored by: Appian

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!

Successful collaboration in the virtual lab

Webinar | Thursday, July 30th | 2pm ET / 11am PT | Sponsored by: IDBS

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!

Proactive Planning: How Supply Chain Risk Mapping Can Prevent Costly Disruptions

Webinar | NOW AVAILABLE ON-DEMAND | Sponsored by: UPS

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 to Watch Now!

Key Scientific Considerations and Concepts in Developing a Global Observational Study Protocol

Webinar | NOW AVAILABLE ON DEMAND | Sponsored by: Parexel

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!

How to Build a TMF Strategy to be Inspection-ready

Webinar | Thursday, April 16th | 2pm ET / 11am PT | Sponsored by: Veeva Systems

Hear how Kythera Biopharmaceuticals reduced their TMF reconciliation time by 40% with their TMF strategy. Sign up for the webinar here.