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Podcasts

Barnett podcasts
The PAREXEL Biopharmaceutical R&D Statistical Sourcebook 2012/2013
Exclusive Interview with Mark Mathieu
Sponsored by Barnett Educational Services
The PAREXEL Biopharmaceutical R&D Statistical Sourcebook is the industry's leading resource for statistics, trends, and proprietary market intelligence and analysis on the biopharmaceutical industry. Supported by thousands of graphs, illustrations, and analyses, the Sourcebook provides the latest intelligence on every aspect of biopharmaceutical development – from product discovery, to R&D performance and productivity, to time-to-market analysis. Mark Mathieu is the Editor of the Sourcebook, and director of strategic research at PAREXEL Consulting. In this interview, he discusses the emerging metrics and benchmarks on the current state and direction of today's biopharm industry, industry activity in clinical development, metrics by therapeutic area, and clinical trials in emerging markets.
Barnett podcasts
Good Clinical Practice Question & Answer Reference Guide, May 2013
Exclusive Interview with Michael Hamrell
Sponsored by Barnett Educational Services
Download this podcast to hear about all new updates to the current Good Clinical Practice Question & Answer Reference Guide, May 2013. Answering hundreds of questions about GCP, the book is the must-have resource for CRAs, investigators/sites, auditors, compliance, legal, and other clinical research professionals. In this podcast, the editor of the book, Michael Hamrell, discusses what's new in the regulatory landscape in 2013, and the latest data and trends on the FDA and EMA's clinical trial compliance inspections, inspectional findings, and common areas of GCP noncompliance.
Barnett podcasts
The HIPAA Privacy Rule and FDA-Regulated Clinical Trials
Sponsored by Exclusive Interview with Sam Sather, MS, BSN, CCRA, CCRC
Happy Birthday, HIPAA! This exclusive podcast is with Sandra "Sam" Sather, MS, BSN, CCRA, CCRC, Founder of Clinical Pathways, LLC. Sam is the author of the GCP Question & Answer Reference Guide's section on "The HIPAA Privacy Rule and FDA-Regulated Clinical Trials." Hear Sam discuss the Omnibus HIPAA Rulemaking and HITECH, as well as strategies for sites, sponsors, CROs, and IRBs.
Barnett podcasts
GCP and Clinical Research Standards in the European Union
Exclusive Interview with Dr. Beat Widler
Sponsored by Barnett Educational Services
This exclusive podcast is with Dr. Beat Widler, the key contributor to this year's GCP Q&A Guide's Chapter on "GCP and Clinical Research Standards in the European Union." Hear Dr. Widler's take on issues such as global outsourcing, the pitfalls and opportunities related to global drug development, and the sharing of protocols and protocol standards across industry.

 Recent podcasts include: 

 

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    Using a Unified Cloud-Based Platform for Clinical Research
 

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     Ride the Wave of Risk-Based Site Monitoring

 
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    Shining Light on Clinical Investigator Cost Budgeting & Planning
 
 

To promote your podcast with Clinical Informatics News or Bio-IT World, please contact:   

 

Jay Mulhern, Manager, Business Development at 781-972-1359 or jmulhern@healthtech.com
 


For reprints and/or copyright permission, please contact  Jay Mulhern, (781) 972-1359, jmulhern@healthtech.com.