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eNewsletters

Issue No. 13

  • Featured Viewpoint: Leveraging strategic partnerships to gain marketplace advantages
  • Industry Perspective:  Q&A with Mario Papillon, VP, Strategic Account Leader
  • Best Practices: Strategic Partnerships


Issue No. 12

  • Featured Viewpoint: Maximizing Product Value in the Era of Comparative Effectiveness Research
  • Industry Perspective: Understanding the Impact of Comparative Effectiveness Research
  • Best Practices: Demonstrating Product Value
     

Issue No. 11

  • Featured Viewpoint: Clinical Logistics Services
  • Industry Perspective: Q&A with Alain Eudaric and Rico Berger
  • Best Practices: Clinical Logistics Services in Emerging Market
     

Issue No. 10

  • Featured Viewpoint: True eClinical: Advancing beyond data integration
  • Industry Perspective: Q&A with Steve Kent, President, Perceptive Informatics
  • Best Practices: Technology in Late-Stage Trials
     

Issue No. 9

  • Featured Viewpoint: eCROs: Delivering the next generation of technology and services for the biopharmaceutical industry
  • Industry Perspective: Q&A with Josef von RickenbachChairman and CEO
  • Best Practices: Five Key Levers
     

Issue No. 8

  • Featured Viewpoint: Understanding the Challenges of Biosimilar Medicines
  • Expert Profile: Cecil Nick
  • Best Practices: Lessons learned from biosimilar development in the EU

 

Issue No. 7

  • Featured Viewpoint: Managing Individual Case Safety Reports for Improved Pharmacovigilance
  • Expert Profile: Dr. John Lambert
  • Best Practices: Understanding the FDA’s Postmarketing Surveillance Program

 

Issue No. 6

  • Cover Story: Exploring New Approaches to Strategic Partnerships
  • Expert Profile: Angelika Riedl
  • Best Practices: Improving Efficiency and Data Access through a Fully Integrated eClinical Platform

 

Issue No. 5

  • Cover Story: Making the Right Imaging Choices for Clinical Trials
  • Expert Profile: Barbara E. Tardiff, M.D., M.B.A.
  • Industry News: Medical Imaging Emerges in Clinical Trials: A 2007 Assessment
  • Best Practices: Evaluating ePRO Tools for Clinical Trials

 

Issue No. 4

  • Cover Story: Global Risk Management: Meeting the Challenge
  • Expert Profile: Anders Neil, Ph.D.
  • Industry News: Postmarketing Study Commitment Trends for New Drugs: An Analysis of NMEs Approved in 2008
  • Best Practices: Accelerating Global Product Introductions Through Multi-country Regulatory Filings

 

Issue No. 3 

  • Cover Story: Industry Agreement Advances Molecular Imaging in Clinical Trials
  • Expert Profile: Denis Miller, M.D.
  • Industry News: Clinical Trial Starts for Oncology
  • Best Practices: Proof of Concept studies help companies save time and money while reducing risk

 

Issue No. 2 

  • Cover Story: Regulatory Challenges in the Asia-Pacific Region
  • Expert Profile: Hans van Bronswijk, M.D., Ph.D.
  • Best Practices: Ethnobridging and the Japanese Pharmaceutical Market
  • Metrics: Trials by the Numbers

 

Issue No. 1 

  • The Beginning of it All
  • Cover Story: Imaging and Neurodegenerative Diseases
  • Expert Profile: James Vornov, M.D, Ph.D.
  • Best Practices: Patient Recruitment

About PAREXEL

PAREXEL is a leading global bio/pharmaceutical services organization that helps clients expedite time-to-market through our development and launch services. These include a broad range of clinical development capabilities, integrated advanced technologies, regulatory affairs consulting, and commercialization services.

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