Should we Leave it to Patients to Identify Counterfeit Medicines?
https://international-pharma.com/wp-content/uploads/2012/04/Pages-from-IPI-V3I3-web-23.pdf
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Editorial Archive
The EU Directive Against Falsified Medicines and the Role of Security Labels
https://international-pharma.com/wp-content/uploads/2012/04/Pages-from-IPI-V3I3-web-22.pdf
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Editorial Archive
Decentral Automation at all Process Levels Intelligent Control Heads Enable Complete Decentral Automation of Hygienic Production Processes
https://international-pharma.com/wp-content/uploads/2012/04/Pages-from-IPI-V3I3-web-21.pdf
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Editorial Archive
Shedding Enhanced Light on Biological and Biomedical Systems
https://international-pharma.com/wp-content/uploads/2012/04/Pages-from-IPI-V3I3-web-20.pdf
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Editorial Archive
Safeguarding the Global Pharmaceutical Supply Chain
https://international-pharma.com/wp-content/uploads/2012/04/Pages-from-IPI-Volume-3-Issue-3-19.pdf
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Editorial Archive
Safely Transporting Clinical Trials through the Middle East
https://international-pharma.com/wp-content/uploads/2012/04/Pages-from-IPI-Volume-3-Issue-3-18.pdf
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Clinical Research v3i3
Modernising Subject Payments in Clinical Trials
https://international-pharma.com/wp-content/uploads/2012/04/Pages-from-IPI-Volume-3-Issue-3-17.pdf
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Clinical Research v3i3
Managing the Use of Research- Grade Kits During Clinical Trials
https://international-pharma.com/wp-content/uploads/2012/04/Pages-from-IPI-Volume-3-Issue-3-16.pdf
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Clinical Research v3i3
Feasibility, Risk Management and Clinical Trials – Art or Science?
https://international-pharma.com/wp-content/uploads/2012/04/Pages-from-IPI-Volume-3-Issue-3-15.pdf
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Clinical Research v3i3
Optimising Clinical Research Site Performance through Additive Patient Enrolment
https://international-pharma.com/wp-content/uploads/2012/04/Pages-from-IPI-Volume-3-Issue-3-14.pdf
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