Date Recorded: 6/22/08Length: 01:48
Size: 2.8MB
Thought Leader: Massimo Raineri, Head of Systems Development - Biometry, Actelion
Massimo talks about the complexity of global drug development.
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Monday, October 6, 2008
DIA 2008 - Actelion
Date Recorded: 6/22/08Length: 01:48
Size: 2.8MB
Thought Leader: Massimo Raineri, Head of Systems Development - Biometry, Actelion
Massimo talks about the complexity of global drug development.
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DIA 2008 - Acurian
Date Recorded: 6/22/08
Length: 01:56
Size: 6.6MB
Thought Leader: Scott Connor, VP, Marketing, Acurian
Scott discusses why patient recruitment remains a major industry challenge.
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Length: 01:56
Size: 6.6MB
Thought Leader: Scott Connor, VP, Marketing, Acurian
Scott discusses why patient recruitment remains a major industry challenge.
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DIA 2008 - Beardsworth
Date Recorded: 6/22/08
Length: 01:06
Size: 3.7MB
Thought Leader: Dan Diaz, VP, Business Development, Beardsworth
Dan says the industry needs to overcome the challenge of enrolling quality subjects into complex trials.
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Length: 01:06
Size: 3.7MB
Thought Leader: Dan Diaz, VP, Business Development, Beardsworth
Dan says the industry needs to overcome the challenge of enrolling quality subjects into complex trials.
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DIA 2008 - Aureus Research Consultants
Date Recorded: 6/22/08
Length: 02:02
Size: 6.9MB
Thought Leader: Alicia Pouncey, Med., Managing Dir., Aureus Research Consultants
Alicia identifies clinical staffing and education as two major challenges.
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Length: 02:02
Size: 6.9MB
Thought Leader: Alicia Pouncey, Med., Managing Dir., Aureus Research Consultants
Alicia identifies clinical staffing and education as two major challenges.
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DIA 2008 - Clinsys
Date Recorded: 6/22/08
Length: 01:22
Size: 2.1MB
Thought Leader: David Williams, CEO, Clinsys
David addresses the need to deliver quality services to industry sponsors.
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Length: 01:22
Size: 2.1MB
Thought Leader: David Williams, CEO, Clinsys
David addresses the need to deliver quality services to industry sponsors.
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DIA 2008 - Clinlogix
Date Recorded: 6/22/08
Length: 01:54
Size: 6.1MB
Thought Leader: JeanMarie Markham, President/CEO, Clinlogix
JeanMarie discusses why the loss of experienced people due to mergers will impact trials.
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Length: 01:54
Size: 6.1MB
Thought Leader: JeanMarie Markham, President/CEO, Clinlogix
JeanMarie discusses why the loss of experienced people due to mergers will impact trials.
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DIA 2008 - CRF
Date Recorded: 6/22/08
Length: 02:35
Size: 9.5MB
Thought Leader: Pamela McNamara, CEO, CRF
Pam outlines five major issues that are impacting the clinical trial space.
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Length: 02:35
Size: 9.5MB
Thought Leader: Pamela McNamara, CEO, CRF
Pam outlines five major issues that are impacting the clinical trial space.
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DIA 2008 - Criterium
Date Recorded: 6/22/08
Length: 01:09
Size: 1.8MB
Thought Leader: Kabelo Pududu, CRA, Criterium
Kabelo says finding investigators for clinical trials is a major challenge.
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Length: 01:09
Size: 1.8MB
Thought Leader: Kabelo Pududu, CRA, Criterium
Kabelo says finding investigators for clinical trials is a major challenge.
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DIA 2008 - CRN
Date Recorded: 6/22/08
Length: 01:40
Size: 5.7MB
Thought Leader: Gail Adinamis, President/CEO, CRN
Gail confirms patient recruitment and retention are still impacting clinical trial efficiency.
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Length: 01:40
Size: 5.7MB
Thought Leader: Gail Adinamis, President/CEO, CRN
Gail confirms patient recruitment and retention are still impacting clinical trial efficiency.
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DIA 2008 - D. Anderson & Company
Date Recorded: 6/22/08
Length: 01:34
Size: 5.3MB
Thought Leader: Melynda Geurts, COO, D. Anderson & Company
Meylnda talks about the challenges involved with the ongoing delays with trials.
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Length: 01:34
Size: 5.3MB
Thought Leader: Melynda Geurts, COO, D. Anderson & Company
Meylnda talks about the challenges involved with the ongoing delays with trials.
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DIA 2008 - DataTrial
Date Recorded: 6/22/08
Length: 01:20
Size: 4.2MB
Thought Leader: Gill Hallet, M.Sc., Dir., European Operations, DataTrial
Gill talks about the need for speed in clinical trials.
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Length: 01:20
Size: 4.2MB
Thought Leader: Gill Hallet, M.Sc., Dir., European Operations, DataTrial
Gill talks about the need for speed in clinical trials.
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DIA 2008 - DSG
Date Recorded: 6/22/08
Length: 01:57
Size: 6.9MB
Thought Leader: Tony Varano, President/CEO, DSG
Tony discusses the need for re-tooling the clinical process.
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Length: 01:57
Size: 6.9MB
Thought Leader: Tony Varano, President/CEO, DSG
Tony discusses the need for re-tooling the clinical process.
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DIA 2008 - etrials
Date Recorded: 6/22/08
Length: 01:58
Size: 6.6MB
Thought Leader: Michael Mickens, VP, Sales and Client Services, etrials
Michael discusses the need for technology integration.
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Length: 01:58
Size: 6.6MB
Thought Leader: Michael Mickens, VP, Sales and Client Services, etrials
Michael discusses the need for technology integration.
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DIA 2008 - Icon
Date Recorded: 6/22/08
Length: 01:49
Size: 2.8MB
Thought Leader: Suzanne Gagnon, M.D., Senior VP, Icon
Dr. Gagnon talks about the public perception regarding drug safety.
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Length: 01:49
Size: 2.8MB
Thought Leader: Suzanne Gagnon, M.D., Senior VP, Icon
Dr. Gagnon talks about the public perception regarding drug safety.
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DIA 2008 - Imperial
Date Recorded: 6/22/08
Length: 01:32
Size: 5.1MB
Thought Leader: Robert McGrath, Sales & Marketing Mgr., Imperial
Bob talks about risk mitigation and why this is a major challenge.
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Length: 01:32
Size: 5.1MB
Thought Leader: Robert McGrath, Sales & Marketing Mgr., Imperial
Bob talks about risk mitigation and why this is a major challenge.
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DIA 2008 - INC Research
Date Recorded: 6/22/08
Length: 02:54
Size: 10.8MB
Thought Leader: Alistair Macdonald, Sr. VP, Data Services, INC Research
Alistair discusses the changing role of CROs.
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Length: 02:54
Size: 10.8MB
Thought Leader: Alistair Macdonald, Sr. VP, Data Services, INC Research
Alistair discusses the changing role of CROs.
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DIA 2008 - Inclinix
Date Recorded: 6/22/08
Length: 02:25
Size: 8.2MB
Thought Leader: Tobin Geatz, CEO and Chairman, Inclinix
Tobin says the drug development process needs to change.
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Length: 02:25
Size: 8.2MB
Thought Leader: Tobin Geatz, CEO and Chairman, Inclinix
Tobin says the drug development process needs to change.
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DIA 2008 - inVentiv Clinical Solutions
Date Recorded: 6/22/08
Length: 01:49
Size: 6.1MB
Thought Leader: Dr. Scott Treiber, Sr. VP, Clinical Operations, inVentiv Clinical Solutions
Dr. Treiber says speed, global development, and staffing are three major issues.
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Length: 01:49
Size: 6.1MB
Thought Leader: Dr. Scott Treiber, Sr. VP, Clinical Operations, inVentiv Clinical Solutions
Dr. Treiber says speed, global development, and staffing are three major issues.
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DIA 2008 - Kendle
Date Recorded: 6/22/08
Length: 01:23
Size: 4.6MB
Thought Leader: Dr. Janet Jones, Director, Feasibility & Patient Recruitment, Kendle
Dr. Jones says shrinking patient pools are affecting recruitment.
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Length: 01:23
Size: 4.6MB
Thought Leader: Dr. Janet Jones, Director, Feasibility & Patient Recruitment, Kendle
Dr. Jones says shrinking patient pools are affecting recruitment.
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DIA 2008 - KForce
Date Recorded: 6/22/08
Length: 01:33
Size: 2.4MB
Thought Leader: Eleanore Doyle, VP, Business Development, KForce
Eleanor says the rising costs of drug development are impacting cycle times.
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Length: 01:33
Size: 2.4MB
Thought Leader: Eleanore Doyle, VP, Business Development, KForce
Eleanor says the rising costs of drug development are impacting cycle times.
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DIA 2008 - Medidata
Date Recorded: 6/22/08
Length: 02:12
Size: 7.5MB
Thought Leader: Ed Sequine, General Mgr., Medidata
Ed believes managing the ever-increasing complexity of the entire pharmaceutical industry is a major challenge.
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Length: 02:12
Size: 7.5MB
Thought Leader: Ed Sequine, General Mgr., Medidata
Ed believes managing the ever-increasing complexity of the entire pharmaceutical industry is a major challenge.
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DIA 2008 - MedPoint Communications
Date Recorded: 6/22/08
Length: 02:08
Size: 7.4MB
Thought Leader: Bill Cooney, President/CEO, MedPoint Communications
Bill talks about the need to improve research productivity to offset the expense of developing new drugs.
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Length: 02:08
Size: 7.4MB
Thought Leader: Bill Cooney, President/CEO, MedPoint Communications
Bill talks about the need to improve research productivity to offset the expense of developing new drugs.
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DIA 2008 - Microsoft
Date Recorded: 6/22/08
Length: 03:01
Size: 10.3MB
Thought Leader: Michael Naimoli, Director, Life Sciences Industry Solutions, Microsoft
Michael says continuing to innovate in a risk-averse environment is a major challenge.
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Length: 03:01
Size: 10.3MB
Thought Leader: Michael Naimoli, Director, Life Sciences Industry Solutions, Microsoft
Michael says continuing to innovate in a risk-averse environment is a major challenge.
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DIA 2008 - Monitorforhire
Date Recorded: 6/22/08
Length: 01:12
Size: 4.2MB
Thought Leader: Scott Freedman, President, Monitorforhire
Scott discusses the need for quality individuals and for training.
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Length: 01:12
Size: 4.2MB
Thought Leader: Scott Freedman, President, Monitorforhire
Scott discusses the need for quality individuals and for training.
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DIA 2008 - Nextrails
Date Recorded: 6/22/08
Length: 01:27
Size: 4.9MB
Thought Leader: James Rogers, President/CEO, Nextrials
James talks about how the increasing costs of drug development are impacting companies.
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Length: 01:27
Size: 4.9MB
Thought Leader: James Rogers, President/CEO, Nextrials
James talks about how the increasing costs of drug development are impacting companies.
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DIA 2008 - Octagon
Date Recorded: 6/22/08
Length: 01:21
Size: 4.5MB
Thought Leader: Jim Walker, CEO, Octagon
Jim discusses the need for processes as a way to increase efficiencies.
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Length: 01:21
Size: 4.5MB
Thought Leader: Jim Walker, CEO, Octagon
Jim discusses the need for processes as a way to increase efficiencies.
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DIA 2008 - Patient Interaction
Date Recorded: 6/22/08
Length: 01:07
Size: 3.7MB
Thought Leader: Bob Loll, VP, Business Development, Patient Interaction (Pi)
Bob talks about the misperceptions surrounding clinical trials and the need to increase the value of the trial process.
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Length: 01:07
Size: 3.7MB
Thought Leader: Bob Loll, VP, Business Development, Patient Interaction (Pi)
Bob talks about the misperceptions surrounding clinical trials and the need to increase the value of the trial process.
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DIA 2008 - Patni
Date Recorded: 6/22/08
Length: 02:28
Size: 8.6MB
Thought Leader: Steve Jolley, VP, Pharmacovigilance, Patni
Steve identifies increasing pressure from regulators to address safety concerns as a major challenge.
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Length: 02:28
Size: 8.6MB
Thought Leader: Steve Jolley, VP, Pharmacovigilance, Patni
Steve identifies increasing pressure from regulators to address safety concerns as a major challenge.
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DIA 2008 - PHT
Date Recorded: 6/22/08
Length: 01:40
Size: 5.5MB
Thought Leader: Sheila Rocchio, VP Marketing, PHT
Sheila says clients are forced to do more with fewer resources.
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Length: 01:40
Size: 5.5MB
Thought Leader: Sheila Rocchio, VP Marketing, PHT
Sheila says clients are forced to do more with fewer resources.
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DIA 2008 - PPD
Date Recorded: 6/22/08
Length: 01:32
Size: 5.0MB
Thought Leader: James Streeter, Executive Dir., EDC, PPD
James discusses how regulatory controls, rising costs, and patient recruitment are impacting large and small companies.
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Length: 01:32
Size: 5.0MB
Thought Leader: James Streeter, Executive Dir., EDC, PPD
James discusses how regulatory controls, rising costs, and patient recruitment are impacting large and small companies.
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DIA 2008 - ProTrials
Date Recorded: 6/22/08
Length: 01:30
Size: 5.0MB
Thought Leader: Jodi Andrews, President/CEO, ProTrials
Jodi identifies the global factors that are impacting clinical research.
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Length: 01:30
Size: 5.0MB
Thought Leader: Jodi Andrews, President/CEO, ProTrials
Jodi identifies the global factors that are impacting clinical research.
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DIA 2008 - Rigel Pharmaceuticals
Date Recorded: 6/22/08
Length: 01:21
Size: 4.4MB
Thought Leader: Theresa Kane Musser, Exec. Dir., Development Operations, Rigel Pharmaceuticals
Theresa talks about the need for excellent science.
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Length: 01:21
Size: 4.4MB
Thought Leader: Theresa Kane Musser, Exec. Dir., Development Operations, Rigel Pharmaceuticals
Theresa talks about the need for excellent science.
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DIA 2008 - SAFE Biopharma Association
Date Recorded: 6/22/08
Length: 01:44
Size: 5.7MB
Thought Leader: Mollie Shields Uehling, President/CEO, SAFE-BioPharma Association
Mollie says the biggest challenge today is getting innovative products to patients faster.
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Length: 01:44
Size: 5.7MB
Thought Leader: Mollie Shields Uehling, President/CEO, SAFE-BioPharma Association
Mollie says the biggest challenge today is getting innovative products to patients faster.
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DIA 2008 - Tech Team
Date Recorded: 6/22/08
Length: 01:11
Size: 3.8MB
Thought Leader: Joanna Gutkowski, Acct. Mgr., TechTeam
Joanna says in light of acquisitions there is a need for cost-effective solutions.
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Length: 01:11
Size: 3.8MB
Thought Leader: Joanna Gutkowski, Acct. Mgr., TechTeam
Joanna says in light of acquisitions there is a need for cost-effective solutions.
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DIA 2008 - Wyeth
Date Recorded: 6/22/08
Length: 01:38
Size: 5.4MB
Thought Leader: Dr. William Jacobson, Dir. Project Mgmt., Wyeth
Dr. Jacobson identifies the enormous changes in the regulatory environment as having a major impact.
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Length: 01:38
Size: 5.4MB
Thought Leader: Dr. William Jacobson, Dir. Project Mgmt., Wyeth
Dr. Jacobson identifies the enormous changes in the regulatory environment as having a major impact.
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Thursday, July 17, 2008
The Clinical Data Liaison: The Key to Better, Faster Clinical Trials
Date: 6/5/2008
Length: 00:05:33
Thought Leader: John Hudak, President and Founder, Criterium Inc.
In this episode, John Hudak talks about the need for a paradigm shift in work flow to improve the clinical trial process and how the evolving role of a centralized clinical data liaison, or CDL, is integral to streamlining data management. Mr. Hudak also discusses how through real-time feedback, the CDL can reduce the number of field monitoring visits required, a major cost in managing clinical studies, and improve overall site efficiency.
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Part of the PharmnaVOICE Industry Vision Series
Length: 00:05:33
Thought Leader: John Hudak, President and Founder, Criterium Inc.
In this episode, John Hudak talks about the need for a paradigm shift in work flow to improve the clinical trial process and how the evolving role of a centralized clinical data liaison, or CDL, is integral to streamlining data management. Mr. Hudak also discusses how through real-time feedback, the CDL can reduce the number of field monitoring visits required, a major cost in managing clinical studies, and improve overall site efficiency.
Go to video
Part of the PharmnaVOICE Industry Vision Series
"Glocalisation" and Your Clinical Trials
Date: 6/5/2008
Length: 00:006:20
Thought Leader: Amanda Decoker, Account Manager, MediciGlobal
Amanda Decoker, discusses how, and why, the business practice of “glocalisation” can be incorporated into the clinical development process, particularly for patient recruitment and retention in global studies. She also outlines the critical elements that are needed to successfully root global programs in local language and culture.
Go to video
Part of the PharmnaVOICE Industry Vision Series
Length: 00:006:20
Thought Leader: Amanda Decoker, Account Manager, MediciGlobal
Amanda Decoker, discusses how, and why, the business practice of “glocalisation” can be incorporated into the clinical development process, particularly for patient recruitment and retention in global studies. She also outlines the critical elements that are needed to successfully root global programs in local language and culture.
Go to video
Part of the PharmnaVOICE Industry Vision Series
Transform While You Perform: The Next Generation of Clinical Operations
Date: 6/5/2008
Length: 00:006:45
Thought Leaders: Nagaraja Srivatsan, Head of Life Sciences, North America, Cognizant
Kaushik Bhaumik, Global Practice Leader, Consulting and BPO, Cognizant
Nagaraja Srivatsan, Head of Life Sciences, North America, Cognizant, Kaushik Bhaumik, Global Practice Leader, Consulting and BPO, Cognizant, discuss the strategies needed to transform the drug development process, the impact of such a shift on a sponsor’s organizational structure, and how transformation differs from operational optimization. They also outline best practices that companies should follow to begin the transformation process.
Go to video
Part of the PharmnaVOICE Industry Vision Series
Length: 00:006:45
Thought Leaders: Nagaraja Srivatsan, Head of Life Sciences, North America, Cognizant
Kaushik Bhaumik, Global Practice Leader, Consulting and BPO, Cognizant
Nagaraja Srivatsan, Head of Life Sciences, North America, Cognizant, Kaushik Bhaumik, Global Practice Leader, Consulting and BPO, Cognizant, discuss the strategies needed to transform the drug development process, the impact of such a shift on a sponsor’s organizational structure, and how transformation differs from operational optimization. They also outline best practices that companies should follow to begin the transformation process.
Go to video
Part of the PharmnaVOICE Industry Vision Series
Making Pharmacovigilance Work: Key steps for implementing a proactive, business-critical safety model
Date: 6/5/2008
Length: 00:06:29
Thought Leaders: Uwe Maennl, M.D., Ph.D., VP and Worldwide Head of Pharmacovigilance, PAREXEL International and Gadi Saarony, Corporate VP and Worldwide Head, PAREXEL Consulting
In this episode, Dr. Maennl and Mr. Saarony discuss a new safety model for pharmacovigilance, including risk management, key stakeholders, and performance benchmarks to this new approach.
Go to video
Part of the PharmnaVOICE Industry Vision Series
Length: 00:06:29
Thought Leaders: Uwe Maennl, M.D., Ph.D., VP and Worldwide Head of Pharmacovigilance, PAREXEL International and Gadi Saarony, Corporate VP and Worldwide Head, PAREXEL Consulting
In this episode, Dr. Maennl and Mr. Saarony discuss a new safety model for pharmacovigilance, including risk management, key stakeholders, and performance benchmarks to this new approach.
Go to video
Part of the PharmnaVOICE Industry Vision Series
Monday, July 30, 2007
accessFYI Overview
Dan Limbach and Enrico DePaolis discuss the launch of accessFYI - The Resource for Life Sciences.
Part of the PharmaVOICE Webcast Network.
Pregnancy Registries in Clinical Trials
Taren Grom, Editor of PharmaVOICE discusses pregnancy registries in clinical trials, with Dr. Deborah Covington, Director of Registries and Epidemiology at Kendle.
Part of the PharmaVOICE Webcast Network.
Technology Integration in Healthcare
Taren Grom, Editor of PharmaVOICE magazine talks with Glen DeVries, Co-Founder and CTO of Medidata Solutions Worldwide, about system integration issues in healthcare.
Part of the PharmaVOICE Webcast Network.
A Paradigm Shift in Pharmaceutical Clinical Trials
Taren Grom, Editor of PharmaVOICE magazine talks with Ira Spector, Vice Chief of Clinical Operations at Wyeth, about improving clinical trials in the pharmaceutical industry.
Part of the PharmaVOICE Webcast Network.
Clinical Development Challenges for Sites
Taren Grom, Editor of PharmaVOICE magazine talks with Jean-Marie Markham, Founder and CEO of Clinlogix, about challenges of sites in clinical development.
Part of the PharmaVOICE Webcast Network.
Exploring the Drug Industry's Therapeutic Focus
Taren Grom, Editor of PharmaVOICE magazine talks with Jim Ogle, CEO of INC Research, about changes in the drug development arena and trends in the industry's therapeutic focus.
Part of the PharmaVOICE Webcast Network.
Staffing Challenges in Clinical Research
Taren Grom, Editor of PharmaVOICE magazine talks with Micheal Hliniak, CEO of InVentiv Clinical, about staffing challenges in the outsourcing arena.
Part of the PharmaVOICE Webcast Network.
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