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Are Your Patient Access Solutions Performing up to Your Expectations? Leveraging data and analytics to enhance performance

Live broadcast: August 6, 2014 from 1-2PM EDT

Patient Access solutions must be supported by rich sources of evidence, demonstrations of convincing payback, and sophisticated predictive models. But how can you tell if your campaign is performing up to expectations?  And if it isn’t, do you have a strategy for mid-course correction? Paul LeVine and Robert Leedom leverage their deep-seated experience in the analytics that drive patient access to show you that you can identify and improve the performance of your patient access solutions through effective mid-course corrections.


Register Free at http://www.pharmexec.com/patientaccess

Sponsor:
TrialCard

 

Seeing the Whole Picture: Harnessing the Power of Data to Drive Smarter Marketing Decisions

Live broadcast: August 7, 2014 from 1-2PM EDT

Learn how big data is revolutionizing how organizations measure the true impact of their digital marketing efforts. Join  leading experts in digital marketing and analytics as they share real-world insights on how new methods of data capture and integration are breaking down current barriers to individual channel analysis and giving marketers the ability to drive real performance improvements. 

Register Free at http://www.pharmexec.com/picture

Sponsor:
Ernst Young

 

ON-DEMAND WEBCASTS NOW AVAILABLE FOR REPLAY

Leveraging Analytics to Inform Payer Messaging: 3 Case Studies

Recorded: June 18, 2014

Market access is a key challenge for Specialty drugs today.  Join Cardinal Health Specialty Solution’s Chief Medical Officer, Dr. Bruce Feinberg, on June 18th at 2:00 PM EST for a provocative discussion of the importance of high-value analytics using real world data to create impactful market messages and ensure brand success.   


Register Free at http://www.pharmexec.com/payermessaging

Sponsor:
Cardinal Health

 

Top 10 Clinical Trial Cost-Cutting Innovations

Recorded: June 26, 2014

Clinical research experts continue to observe the rising costs and reduced efficiency of clinical studies. At the same time, today’s evolving healthcare landscape prioritizes empowering the patient. This combination has resulted in clinical research shifting towards a patient-centric model. Understanding these changes and implementing appropriate strategies is vital to improving outcomes.

Join the discussion as Ms. Erem Latif, Trial Enhancement Services, UBC, will share proven innovative and cost-cutting strategies to maximize the efficiency and effectiveness of clinical research.

Register Free at http://www.pharmexec.com/top10

Sponsor:
UBC Express Scripts

 

Methods for patient-centered endpoint selection in rare disease drug development programs

Recorded: July 23, 2014

While stakeholder groups have called for patient engagement in rare disease drug development programs, traditional methods for engaging patients in endpoint strategy are very often impossible due to the nature of rare diseases.  This webinar will review innovative methods for gathering patient input to inform endpoint selection and provide specific examples of successful solutions.

Register Free at http://www.pharmexec.com/endpoint

Sponsor:
Evidera

 

How Digital Medicine Can Pinpoint Dosing Regimens to Optimize Drug Efficacy and Safety

Recorded: May 14, 2014 from 11-noon Eastern

Attend this webcast to discover how innovations in digital medicine and electronic data capture enable accurate and timely insight into medication adherence during a clinical trial – helping to determine optimum dosing ranges and reducing clinical trial attrition, especially in Phase III trials. 


Register Free at http://www.pharmexec.com/pinpoint

Sponsor:
Oracle

Multi-faceted Approaches to Meet Payer and Regulatory Evidence Requirements

Recorded on: March 19, 2014

Challenged by the need to gather real-world evidence to meet post-marketing payer and regulatory evidence requirements?

Dr. Janine Collins, Senior Director, European Risk Management, and Krista Payne, Executive Director, Sr. Research Scientist, Value Demonstration, will share current perspectives, opportunities, and challenges in relation to the impact of converging payer and regulator evidence requirements on PASS and PMR studies.


Register Free at http://www.pharmexec.com/evidence

Sponsor:
UBC Express Scripts

 

Overcoming the Life Sciences Content Conundrum in a Multichannel World
Recorded on: March 5, 2014

A must attend webinar for life sciences companies who are serious about driving a successful multichannel strategy by overcoming their promotional content challenges through a smarter end-to-end content management approach.  Hear from our experts, Jan van den Burg, VP Commercial Strategy at Veeva Systems and Chris Moore, Partner at Ernst & Young and Life Sciences Content Management & Analytics Expert. Learn  about the key factors for successful execution and the benefits you stand to gain, including enhanced marketing and brand cooperation, better scaling of content both globally and locally, remaining compliant across channels, all whilst lowering costs.


Register Free at http://www.pharmexec.com/multichannel

Sponsor:
Veeva

New Industry Research: Transforming Clinical R&D Strategy and Performance with Real-World Data
Recorded on: February 13, 2014

Join speakers from the Tufts Center for the Study of Drug Development, Oracle Health Sciences, and Context Matters to explore how protocol and trial designs can be optimized not only for greater R&D efficiency but also to discover health economic outcomes with clinical outcomes. 


Register Free at http://www.pharmexec.com/performance

Sponsor:
Oracle

 

Evaluation of EU Post-Authorization Safety Studies Using Recent EU-RMP Summary Data: Analysis, Trends, Implications
Recorded on: January 29, 2014

This Webcast will provide an overview of recent trends in EU PASS, including an analysis of a sample of EU-RMP summary data, description of PASS types requested and comparison/contrast of characteristics between drug types.

Implications for Pharmaceutical Companies and lessons learnt will be discussed


Register Free at http://www.pharmexec.com/eu_rmp

Sponsor:
Evidera

 

Pre-Approval Risk Mitigation Strategies and Proactive Safety Considerations
Recorded on: December 10, 2013

Discover ways biopharmaceutical companies can proactively prepare during drug development to monitor and assess patient safety in the postapproval period.


Register Free at http://www.pharmexec.com/preapproval

Sponsor:
UBC Express Scripts

 

An Intro to Utility Assessment Methods
Recorded on: December 5, 2013

This webinar will provide an introduction to utility theory and utility assessment methods with select case studies, in addition to a discussion of the influence of the National Institute of Clinical Excellence (NICE) on utility assessment. We will focus on direct utility assessment, indirect utility assessment (multi-attribute measures and condition – specific measures), deriving utilities from condition-specific measures, and mapping methods.


Register Free at http://www.pharmexec.com/utility

Sponsor:
Evidera

 

Avoid the Last Minute Rush-Planning Ahead for Successful Global Market Access
Recorded on: November 20, 2013

Successful market access is never easy, but waiting too long to plan for it can make life harder than it need be. In our experience, while there are companies that plan well, too few do this at the right time in the product development lifecycle. There are always difficult questions to be addressed and a range of uncertainties that must be considered in approaching global market access and the associated evidence generation activities. In this webcast, we:

  • Highlight some of the common pitfalls to avoid
  • Outline a process that will ensure key questions are addressed (but won’t guarantee commercial success!)
  • Provide case studies to illustrate sensible planning for evidence generation activities


Register Free at http://www.pharmexec.com/rush

Sponsor:
Evidera

 

Oncology Data Management Innovations
Recorded on: November 20, 2013

Join us for a webinar highlighting innovations in data and information management specifically for Oncology. Oncology commercial teams today continue to face several important issues, including data gaps due to specialty distribution, small patient counts at local levels, integrating data across infusion and pharmacy channels, understanding product usage across multiple indications, and more.


Register Free at http://www.pharmexec.com/datamgmt

Sponsor:
ZS Associates

 

Let the Sunshine In: What Executives Need to Know as the Open Payments Program is Fully Implemented
Recorded on: November 14, 2013

Life Sciences companies must constantly identify and monitor the corporate, reputational, and personal liability risks inherent in their worldwide business activities. The Open Payments program has placed a renewed focus on the relationship between the Life Sciences industry and the healthcare provider community. While the intent of the law is to provide direct insight and transparency into these relationships, the data will ultimately serve as a tool to identify non-compliance by regulators, business intelligence by competitors and potentially controversial analyses by the media - ultimately exposing the company to greater risk across the board. The time to act is now—companies ahead of the pack are considering the various types of scenarios that could potentially increase corporate and executive risks and they are taking action.


Register Free at http://www.pharmexec.com/openpayments

Sponsor:
Huron Life Sciences

 

Pharma's Shift to Custom Solutions Marketing
Recorded on: October 31, 2013

eHealthcare Solutions, experts in digital healthcare marketing with vast experience in building programs that drive results, shares insights about the latest options in custom digital programs targeting physicians/HCPs.

Hear these innovators provide tips on:

  • Invigorating your marketing campaigns
  • Engaging highly valuable audiences at the right time
  • Achieving Maximum Brand Impact and measurable ROI

Register Free at http://www.pharmexec.com/custom

Sponsor:
e-Healthcare Solutions

Integrated Strategies for Oncology Provider Engagement
Recorded on: October 30, 2013

During this presentation, we will examine how industry trends are impacting the way Pharmaceutical and Biotech companies interact with physicians, and how to implement strategies to optimize engagement with providers. Specifically, we will discuss:

• Key industry trends impacting oncology providers
• How to implement strategies that foster strong relationships with providers
• New approaches to deliver relevant and timely information to providers


Register Free at http://www.pharmexec.com/provider_engagement

Sponsor:
McKesson

 

Improving Clinical Trial Management with cloud-based eTMF


Join industry thought leaders, Rik van Mol of Veeva Systems and Eldin Rammell as they share valuable insights on how you can improve your clinical operations efficiency to significantly improve your clinical trial management process. Leading functional CRO, International Drug Development Institute (IDDI), will share their thoughts on how a cloud-based eTMF solution is helping improve their quality and document management processes and enhancing audit management.


Register Free at www.pharmexec.com/etmf

Sponsor:
Veeva

 

Rare diseases: Evidence, Value, Insight
Recorded on: October 2, 2013 / 10:00am - 11:00am EDT

The past decade has seen numerous innovations in novel therapies for rare diseases, providing clinical and humanistic benefits for populations that are small but have large unmet need. Payers and manufacturers alike recognize the high price of innovation, and healthcare systems have struggled in recent years to manage the budget impact of life-changing treatments for patients with rare diseases


Register Free at www.pharmexec.com/raredisease

Sponsor:
Evidera

 

Increase the Value of Database Research with Validated Coding Algorithms
Recorded on: September 18, 2013, 10:00EDT

In today?s research environment, the employment of high quality methods for retrospective database research has never been more relevant. Database publications continue to significantly increase over time for both claims database and electronic medical record (EMR) database studies, and initiatives such as the Observational Medical Outcomes Partnership (OMOP) and Mini-Sentinel as well as large safety-based studies in the U.S. and Europe have focused their efforts in the area of epidemiological and safety-based research. This webinar will focus on the how the identification and development of validated coding algorithms are used in defining study cohorts, health outcomes of interest, as well as patient comorbidities, and the opportunities and challenges of using these algorithms in database research.


Register Free at www.pharmexec.com/increase

Sponsor:
Evidera

 

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