Recent Advances in Multiple Myeloma and Their Implications for Future Development
March 29, 2018 | 11am ET / 8am PT | SmartAnalyst

The webinar discussion will focus on important topics for Hemato-Oncology commercial and clinical development teams, including how treatment strategies in Multiple Myeloma are evolving, and why recent advances in the field will shape strategies for differentiation and value. Register Now

Container Closure Integrity: Six Keys to Simplify Your Strategy and Execution
March 27, 2018 | 11am PT / 8am PT | West Pharmaceutical Services

Looking to clarify and simplify your CCI approval? Although CCI is a very complex issue, the right approach can simplify it. This webinar will provide six key areas to consider in view of Chapter <1207> that enable a holistic approach to optimize sterile product package CCI, and a comprehensive approach to optimizing CCI, including an understanding of the impact of materials, equipment, process, measurement, and more. Register now!

Optimize and Transform Clinical Oncology Research
March 20, 2018 | 12pm ET / 9am PT | Medidata

Discover how increasingly sophisticated technology with advanced analytics is helping clinical investigators and trial leaders overcome certain challenges, and learn how a data-driven approach is a catalyst for optimal study design, improved site selection, and more. Register now!

Not Just Tiny Humans: Conducting Pediatric Clinical Trials
Tuesday, March 13 | 1pm ET/10am PT | Rho

When it comes to the conduct of pediatric clinical trials, there are a number of things you need to consider in order to ensure the successful conduct of a study. From study design to logistics to recruitment, this webinar will look at the key differences between studies conducted in pediatric populations and studies conducted in adult populations. Register now.

Using Product Ideation to Achieve Commercial Success
March 8, 2018 11am ET / 8am PT | Camargo

This webinar will benefit Investors and executives at Biotech and Pharma companies interested in increasing portfolio value through Product Ideation, an often-overlooked creative process utilizing the 505(b)(2) pathway that drives innovative products to market with lowest cost, time, and risk. Register Now

How a Good Regulatory and Computational Strategy Helps Avoid Common Pitfalls
Tuesday, March 6 | 2pm ET / 11am PT | Applied Biomath

The development of New Chemical and Biological Entities is becoming more and more challenging. 

Join Dr. Lorna Speid and Dr. John Burke for this webinar as they discuss:

  • how to develop a Regulatory Strategy
  • case studies on how Model-Aided Drug Invention can support regulatory strategy
  • and more

Register now.

2018 US Customer Reference Data Survey

Companies rely on data about healthcare professionals (HCPs), healthcare organizations (HCOs), and their affiliations to manage customer engagement and ensure compliance. 

The 2018 US Customer Reference Data Survey examines the current state of customer reference data in life sciences through the opinions and experiences of industry executives across the United States. Respondents will be entered for a chance to win one of 3 $50 Amazon gift cards. Take the survey now!


Learn How Med Dev Companies Make Better Data-Driven Decisions
Wednesday, February 28 | 12pm ET / 9am PT | Medidata Solutions

Global wearable device traffic is expected to surpass 40 zettabytes by 2020...one zettabyte equals 1 trillion gigabytes. And this big data explosion is just as apparent within clinical trials. 

Learn how data-driven decision-making solutions based on evolving technology are influencing strategies for managing risk, quality and performance management. Register now.

Is Your Clinical Supply Playbook Ready for Phase II and Beyond?
February 27, 2018 | 11am ET / 8am PT | Catalent

During this webinar, experts from Catalent will discuss:

  • How clinical supply and the supply chain change as a program progresses through Phase I, Phase II and Phase III
  • Which study characteristics contribute most significantly to clinical supply complexity and with these identified, how to build an informed and proactive supply strategy
  • How regulatory and quality requirements can vary by region and what you can do to prepare to meet them
  • Important clinical supply quality considerations when running studies in regions undergoing significant regulatory changes. 

Register here!

Phase Appropriate Stability Studies in Pharmaceutical Development
February 22, 2018 | 2pm ET / 11am PT | Catalent

Join an industry expert in this webinar for key insights on stability testing to support various stages of development and regulatory filings (IND, NDA and ANDA). Register here. 

Medical Device Innovation: Are You Outrunning The Competition?
Reprints Desk

The competitive landscape in medical device R&D is tough. And simply investing in R&D is no guarantee for profitability. So how do you accelerate time-to-market?

Read this white paper and learn why:

  • Mastering the knowledge complex is key to profitability
  • Realizing knowledge efficiences can enable market success
  • Simplifying literature access improves product innovation
Is Your Life Science Data “F-A-I-R”?
Now Available On-Demand | Dell EMC

Is Your Life Science Data “F-A-I-R”? Join DataFrameworks & Dell EMC in this webinar to discover a new approach to create scientific data that is findable, accessible, interoperable, and reusable. Register now!

How Life Sciences Companies Use Box for Regulated Content in the Cloud
Box and USDM Life Sciences

Biopharma and medical device companies can now collaborate on, manage and distribute regulated clinical, lab and manufacturing content in Box. That means all of your content is standardized on a single content repository that meets regulatory and compliance standards, so you can eliminate inefficient silos, enable seamless collaboration and accelerate the validation process.  Combining Box with the power of USDM’s Cloud Assurance (Continual Validation), you will never need to worry about validation again. Read more.

[Whitepaper] CFO's, Is This Part Of Your Corporate TO DO List?
RBC Wealth Management
  • Employee stock option trading & administration
  • Restricted stock transactions (Rule 144)
  • Affiliated trading plans (10b5-1)
  • Directed share plans (friends & family list)
  • Equity comp plan administration — private to public

Guiding corporate executives through regulatory complexities, while delivering an array of sophisticated investment options. Learn more.

Atrium Innovations: Modernizing Quality Operations With Cloud
Now Available On-Demand | Veeva

Atrium Innovations, an innovative leader in the development, manufacturing, and commercialization of science-based nutritional health products, is leveraging cloud technology to bring together 13 sites around the world and multiple functional groups. Register Now to learn more about cloud technology.

Executive Summary
Why Formulation Technologies are Critical to the Success of the Next Generation of Small Molecule Drugs

By taking advantage of modern screening technologies, drug developers can bridge the gap between molecule discovery and dose form selection with Parallel Screening. This executive summary delves into how this method is the most efficient way of maximizing a NCE’s chances of making it to Phase 1. Download it now!

Insights and Key Strategies for Steering Your Biosimilar to Regulatory Success
Recorded on Tuesday, January 23, 2018 | 11am ET / 8am PT | Cardinal Health

Join Cardinal Health Specialty Solutions as we review the biosimilar landscape and identify key strategies for overcoming regulatory barriers and getting your biosimilar to market quickly.

Register now!

PwC Health Research Institute's Top health industry issues of 2018
Thursday, January 18 | 1pm ET / 10am PT | PwC

In 2018 healthcare leaders will be adjusting their strategies to focus on investments, collaborations and efficiencies that build enterprise resilience on a baseline of continued uncertainty. Discover the risks and uncertainties are moving to center stage next year. Register now!

Tufts eClinical Landscape Study: Q&A with Industry Experts
Recorded on January 16, 2018 | Veeva

Hear expert analysis of the 2017 eClinical Landscape Survey, one of the largest, most in-depth surveys of clinical data management professionals that shows the impact of database build delays on trial timelines, as well as the projected increase of data source usage. Register Now.

Bench to Clinic: Preparing for a Successful Transition
Recorded on Wednesday, January 17, 2018 | 1pm ET / 10am PT | Rho

Getting a new product from the bench into the clinic is a complex endeavor.  This webinar will provide an overview of the clinical, nonclinical, CMC, and regulatory activities necessary for a successful IND submission. Register Now.