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.

If you are interested in submitting items to the Library, please contact our advertising team

WEBINARS

The Library is currently filtered to only show Webinars. You can remove this filter by returning to the Library.

The Basics of Biotech 101, 201 & 301

Webinar | Price: $299

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.

Analytic Methods for Identifying Quality Risks in Clinical Trials

Webinar | February 17, 2016 | 11am ET / 8am PT | Presented By: Medidata

Join this webinar on analytic methods to help you minimize regulatory review cycles. Learn how automated systems are using advanced statistical algorithms and machine learning techniques to help sponsors shave months off their quality audit processes and avoid deficiencies. Reserve Your Spot Today!

Rare Disease 20/20: A Look at the Challenges and Opportunities in Rare Disease Clinical R&D

Webinar | Tuesday, February 23 | 2pm ET / 11am PT | Presented By: BBK Worldwide

Join the National Organization for Rare Disorders (NORD), Xenon Pharmaceuticals and BBK Worldwide as they take a closer look at the challenges and opportunities in rare disease clinical R&D. Registration is free – click here.

Special Considerations for Managing Immuno-oncology Studies - A New Paradigm

Webinar | March 9 | 11am ET / 8am PT | Presented by: Medpace

Immuno-Oncology Webinar: We are in a new era for researching cancer treatments. Join Medpace medical and operations experts as they discuss the unique considerations for managing immuno-oncology studies as well as insights into best practices. Register now!

Physician Prescribing Trends & Opportunities for Health System-Pharma Collaboration

Webinar | Wednesday, March 16 | 11am ET / 8am PT | Presented By: athenahealth

athenahealth conducted a study to learn how health systems and new reimbursement models are impacting prescribing behavior. We'll discuss our findings, including opportunities for pharma marketers, with a health system leader during this webinar. Reserve Your Spot Today!

Life Sciences and Mobile Apps

Webinar | March 17 | 1pm ET / 10am PT | Sponsored By: Appian

This webinar will examine app strategies in the life sciences industry and how they're changing in the wake of new regulatory requirements. Register Now!

Drug Manufacturing Solutions in a Complex Industry

Webinar | Now Available On-Demand | Presented by: Catalent

Through expert content and case study examples, this webinar will focus on flexible manufacturing solutions to address the unique needs of today’s pharmaceutical pipelines, with an emphasis on successful technology transfer and tailored manufacturing services. Register to watch now!

Literature Surveillance in Pharmacovigilance; Current Trends, Methods and Challenges

Webinar | Now Available On-Demand | Presented By: Elsevier

Scientific and medical literature is an important source of information to identify suspected adverse reactions with medicines. Join us to learn more about drug safety and literature monitoring for pharmacovigilance. Register to watch now!

Protocol Design: What You Need to Know to Ensure a Successful Study

Webinar | Now Available On-Demand | Presented by Rho

Solid protocol design is critical to clinical development. No matter how well executed a clinical study is, if the underlying design is flawed, it wasn't worth doing. In this webinar, David Shoemaker, SVP R&D, will point out common mistakes and challenges associated with developing a protocol. Register to watch now!

Optimizing Your Clinical Supply Chain Strategy for Asia-Pacific Studies

Webinar | Now Available On-Demand | Presented by: Catalent

In this webinar we will explore how to leverage the major clinical supply centers of China, Singapore and Japan to support clinical trials within the Asia-Pacific region for both local and global study sponsors. We will explore clinical packaging, logistics and import/export considerations that should be taken into account when developing a clinical supply strategy and why there is no substitute for on-the ground local expertise. Register to watch now!

Quality Documentation Control: How to Move From Paper to Regulated Cloud in 4 Weeks

Webinar | Now Available On-Demand | Presented by Veeva

How do you maintain control over regulated content with a mobile and global team? Learn how Medicines360, a nonprofit company, moved from paper-based to electronic content processes in just 4 weeks with Veeva Vault QualityDocs. Register to watch now!

Fastest Route to Clinic and Market Enabled by Optimizing API Properties and Formulation

Webinar | February 24 | 10am ET / 7am PT | Presented by: Catalent

The clinical and commercial success of a new chemical entity (NCE) requires pre-formulation studies of drug candidates and development of suitable formulations based on the physicochemical and biopharmaceutical properties. Through expert content and case study examples, this webinar will highlight the strategies and state-of-art screening, particle size reduction and formulation technologies to optimize the properties and formulation of your drug candidates. Register now!

Improving Commercial Content Compliance & Productivity: Results from New Industry Survey

Webinar | Now Available On-Demand | Presented by Veeva

Discover new trends and strategies to improve compliance and marketing productivity. See how your organization compares. Register to watch now!

Capturing the Voice of the Patient - ePRO, Real World Data, and the Future of Clinical Trials

Webinar | Now Available On-Demand | Presented By: Medidata

Regulators are becoming wary of self-assessments captured on paper, so join this session to learn what is currently driving ePRO decisions. Register to Watch Now!

Enhancing the Customer Experience with Engaging Patient Services Applications

Webinar | Now Available On-Demand | Presented By: Salesforce

Patients increasingly have more control over their healthcare and information, and expect support services, access to their data, and anytime engagement. Join Harvey Guindi and Arun Bhaskar from Health Network Laboratories to hear how they transformed their patient relationships with an engaging suite of applications built on the Force.com platform. Register to Watch Now!

Moving Along the TMF Maturity Continuum

Webinar | Now Available On-Demand | December 10th, 2015

Join us for this webinar to learn how the Veeva TMF Maturity Model for Life Sciences can help you evaluate your TMF operating model and create a strategy that propels your organization along the TMF continuum. Register to watch now! 

Supporting Data Integration for Translational Research with Sustainable Technology Infrastructure

Webinar | Now Available On-Demand | Presented By: PerkinElmer

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. Register to View Today

What's in Your Lab? Address Risk, Cost & Productivity with Chemical Inventory Management

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

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!

What's in Your Lab? Address Risk, Cost & Productivity with Chemical Inventory Management

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

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!

mHealth, the Next Revolution in Clinical Trials

Webinar | NOW AVAILABLE ON-DEMAND | 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 to Watch Now!

UDI Class II Device Submissions: What You Need to Know

Webinar | NOW AVAILABLE ON-DEMAND | Presented by: Reed Tech

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.

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!

'