PharmExec Webcasts

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Avoid the Last Minute Rush – Planning Ahead for Successful Global Market Access

Live broadcast: December 17, 2014 at 10AM ET
Do you have market access challenges (e.g. evidence generation planning) that you are facing, or might face in the next few years?  Join Terry Wilcox, Senior Research Leader, and Clark Paramore, Vice President, for Evidera insights into planning for successful global market access.

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

Sponsor:
Evidera

 

Best Practices for a Successful Global Access Program

Live broadcast: January 12, 2015 at 11AM ET
Join us as Clinigen and Cubist present best practices for developing and implementing a Global Access Program.  Learn how to engage the right stakeholders, operate within the regulatory framework and help patients in need.

 

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

Sponsor:
Clinigen

 

 

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Enhancing Patient Engagement - How to Maximize Nursing and Adherence Solutions

Recorded: November 20, 2014

Every day, pharmaceutical companies are challenged to develop cohesive patient support programs that properly engage patients throughout their experience with a product. Discover how you can benefit from recognizing the questions you should be asking and what you can do to keep patients engaged at every point of their health journey and your product lifecycle. Proven customized clinical programs that can help increase adherence will be discussed.

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

Sponsor:
UBC Express Scripts

 

Market Access for Orphan Drugs in China

Recorded: November 18, 2014

A significant number of patients in China have rare / orphan diseases. As the priority of China’s health care reform recently moved to increase the depth of coverage, the number of critical diseases and the percentage of reimbursement by the state continue to increase. In this webinar, we will share with you the opportunities and challenges for orphan drugs to gain access to the patients in China and what a manufacturer could do to prepare for market access in China. 

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

Sponsor:
Evidera

 

Establishing Processes and Controls to Ensure an Inspection-ready TMF Every Day

Recorded: October 1, 2014

The MHRA recently updated its definition of a critical GCP finding to include TMFs that are not readily accessible or incomplete. It is difficult to achieve the right level of control and accessibility without the proper technology. Join PharmaStart’s Rebecca Moraris and Veeva’s Mike Burton to hear how PharmaStart implemented Veeva Vault eTMF to automate critical processes and provide their partners remote access to the TMF.

 

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

Sponsor:
Veeva

 

New expensive treatments for hepatitis C infection: have US payers reached a tipping point?

Live broadcast: September 24, 2014 at 10AM EDT

The launch of Sovaldi® (sofosbuvir, Gilead) in the US earlier this year marked an important advance in the treatment of hepatitis C virus (HCV) infection, but its price –at $84,000 for a 12-week treatment course – has come under heavy scrutiny. Although downstream cost savings mean that Sovaldi® represents good value to payers over the long term, the product finds itself at the center of a growing debate about the future of drug pricing and cost containment in a health system struggling to cope with the escalating costs of specialty medications.

In this webinar, we ask if recent experience with HCV treatments would suggest payers have reached a tipping point in terms of their willingness or ability to accept high-priced, specialty drugs. We will examine the key dynamics in the HCV market, actions already taken by US payers to contain HCV treatment costs, what further strategies could be considered (taking the practicalities of the US system into account), and future implications for high-cost treatments.

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

Sponsor:
Evidera

 

Engineer Your Business to Win in the Mobile Selling Moment

Live broadcast: September 25, 2014 at noon EDT

Mobile moments -- the expectation I can get what I want, anytime, in my immediate context -- is the new battleground for engaging employees and healthcare providers. If you're not there to provide an instant answer, you’ll lose.

Join guest speaker Ted Schadler of Forrester Research, Inc. as he outlines how to engineer your business to win the mobile moment. Also learn how Stryker Medical leapt ahead of the competition with mobile selling moments for their sales reps.

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

Sponsor:
Prolifiq

 

Establishing Processes and Controls to Ensure an Inspection-ready TMF Every Day

Live broadcast: October 1, 2014 at 2pm EDT

The MHRA recently updated its definition of a critical GCP finding to include TMFs that are not readily accessible or incomplete. It is difficult to achieve the right level of control and accessibility without the proper technology. Join PharmaStart’s Rebecca Moraris and Veeva’s Mike Burton to hear how PharmaStart implemented Veeva Vault eTMF to automate critical processes and provide their partners remote access to the TMF.

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

Sponsor:
Veeva

 

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

Recorded: August 6, 2014

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

Recorded: August 7, 2014

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

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