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Marken Expands Regulatory And Technical Excellence In Logistics
Date:1/30/2013

RESEARCH TRIANGLE PARK, N.C., Jan. 30, 2013 /PRNewswire/ -- Marken today announced the expansion of its internal regulatory and technical expertise with the promotion of Dan Bell to Vice President.  The announcement follows an industry-led panel discussion hosted by Marken in Farmingdale, New York on January 15th.  The panel was convened to shed light on the growing complexity of clinical supply chain management.  Industry experts shared a wide range of perspectives relating to clinical trials risk, cost, resources and security.

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Rafik Bishara , Ph.D., current Chair of the Pharmaceutical Cold Chain Interest Group (PCCIG) within the Parenteral Drug Association (PDA), said: "There is a very clear shift in how we should view 'cold chain' logistics, especially with the growth of biologically derived drugs and vaccines.  Supplier's Quality Systems will need to be expanded to include increased tracking for chain of custody assurance, more reliable data monitoring and compliance with changing customs requirements in developing countries. This shift will go far beyond our current understanding and application of Good Distribution Practices."  The panel was moderated by Pfizer's Bruce Guenter , who said: "Our industry will certainly demand more reliable monitoring of data and will need to ensure compliance with the changing regulations.  It is vital to our industry that we continue to coordinate collaborative exchanges like this to ensure that we are ready, prepared, and ahead of the curve." 

Marken has long been known for its high quality, compliant and reliable service to the pharmaceutical industry.  A new unit has been formed,
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