Global Standards for Identification: Untapped Opportunities in the Clinical Supply Chain
Jesper Franke, Head of Healthcare, GS1 Denmark, explains how the industry can best...
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Elucidating Opportunities for Cost Reduction of Clinical Trials Through Supply Management Optimization
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![shutterstock_584491714]()
Industry Viewpoints: Digitizing Clinical Manufacturing
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![shutterstock_151231130]()
Early Phase Trials: Streamlining Your Biologics Process to Optimize Supply
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![shutterstock_676666975]()
The Brexit Clock is Ticking, Are You Ready?
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![shutterstock_194807486]()
Industry Viewpoints: Investigator-Initiated Studies – A Challenge for Supply with IMPs?
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![shutterstock_242481727]()
Serialization of Prescription Drugs: Readiness from Development into Commercialization
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Global Standards for Identification: Untapped Opportunities in the Clinical Supply Chain
Jesper Franke, Head of Healthcare, GS1 Denmark, explains how the industry can best improve supply chain processes by adopting industry standards
Elucidating Opportunities for Cost Reduction of Clinical Trials Through Supply Management Optimization
Anthony Zuccarello, Associate Director, IRT and Global Clinical Supply Strategy, Amicus Therapeutics, offers insight on how to create efficiencies within the clinical supply chain
Industry Viewpoints: Digitizing Clinical Manufacturing
Clive E. Badman, OBE, talks to CTA’s Charlie Abrines about the digitization of the clinical supply chain
Early Phase Trials: Streamlining Your Biologics Process to Optimize Supply
Jonas Fransson, Director Drug Product Development, Swedish Orphan Biovitrum AB, shares the steps and activities to get your biological clinical trial material ready
The Brexit Clock is Ticking, Are You Ready?
With Brexit only months away, CTA’s Charlie Abrines explains why the pharmaceutical industry should prepare for the worst
Clinical Trials in the US Midwest: Looking Back
As OCT & CTS Midwest gets underway, CTA pays tribute to previous articles written by authors from the US Midwest
Industry Viewpoints: Investigator-Initiated Studies – A Challenge for Supply with IMPs?
Peter Orosz, Head of Clinical Supply Chain Management & Oncology, Boehringer Ingelheim, addresses the challenges of investigator-initiated clinical trials
Serialization of Prescription Drugs: Readiness from Development into Commercialization
Hector Tamburini, Exec. Director, Regulatory Affairs & CMC, Prometheus Laboratories, examines how the industry needs to comply with regulations concerning serialization
The Million Dollar Question – How can Technology Improve Efficiency in the Clinical Supply Chain?
Rey Bacchus, Clinical Trial Supply Manager, Janssen Pharmaceutical R&D, examines what impact novel technology will have on supply chain processes
Expert Insights: Serialization is a Necessary Step to Pharma Industry’s Adoption of Blockchain
Peter Shapiro, Editor-In-Chief, PharmSource, guest writes for CTA and examines how serialization is key to a wider adoption of blockchain in pharma
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