Pharma Logistics Applications & Studies
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Total Transportation Management Saves Company $10.2 Million
9/20/2018
A leading multinational pharmaceutical company with an extensive clinical trial pipeline needed to achieve a comprehensive, fully-managed transportation strategy. Learn more about an outsourced transportation option that delivered tangible results.
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Temperature Control Distribution EU Product Launch
1/10/2018
A US biopharmaceutical company approached Almac to assist with the EU product launch of their high value, temperature sensitive, orphan drug product.
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Case Study: Simplifying Data Management In A Complex Study
5/11/2011
For a Global trial, our customer worked with multiple players, including affiliates and an external CRO.
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Data Driven Market Success
5/11/2011
A Quintiles customer needed an experienced post-marketing ally who could plan for the unknown and design an observational study to eventually include several affiliates, thousands of sites, and more than 55,000 patients, with start-ups staggered over time.
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Aptuit Blister Packaging Case Study
4/28/2011
A client, in need of global blister packaging, had received an exorbitant estimate from a Clinical Packaging and Logistics provider other than Aptuit.
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Case Study: Comprehensive Preclinical Development Program
4/9/2010
Aptuit was asked to conduct an extended package of preclinical studies within a short time frame. As the critical studies are dependent on the results of earlier work in the package (for example, initiation of the 28 day toxicology studies are dependent on the completion of bioanalytical method development, dose range finding, etc.) not only scheduling, but adherence to the schedule was the major risk to achievement of the overall aim, and on time filing to the regulator. By Aptuit, Inc.
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Comprehensive Preclinical Development Program
4/9/2010
Aptuit was asked to conduct an extended package of preclinical studies within a short time frame. As the critical studies are dependent on the results of earlier work in the package (for example, initiation of the 28 day toxicology studies are dependent on the completion of bioanalytical method development, dose range finding, etc.) not only scheduling, but adherence to the schedule was the major risk to achievement of the overall aim, and on time filing to the regulator. By Aptuit, Inc.
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Case Study: Product Development Of An Inhaled Protein
4/9/2010
A small biotechnology company in the United States turned to Aptuit to support the development of their inhaled respiratory product. They had added confidence that their limited in-house capability would benefit from Aptuit’s substantial experience and capabilities in respiratory science projects, fulfilling their need for first-in-class capabilities in manufacturing, clinical packaging and logistics, bio-analytics and respiratory analytics. By Aptuit, Inc.
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Product Development Of An Inhaled Protein
4/9/2010
A small biotechnology company in the United States turned to Aptuit to support the development of their inhaled respiratory product. They had added confidence that their limited in-house capability would benefit from Aptuit’s substantial experience and capabilities in respiratory science projects, fulfilling their need for first-in-class capabilities in manufacturing, clinical packaging and logistics, bio-analytics and respiratory analytics. By Aptuit, Inc.
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Case Study: Controlled Drug Handling
4/9/2010
A midsize pharmaceutical company came to Aptuit to work through the complexities of exporting a controlled substance manufactured in the United States and an EU-sourced comparator for inclusion in a clinical trial across more than 12 EU participating countries. Aptuit’s client was dealing with an Investigative Medicinal Product (IMP) manufactured in the United States and an EU-sourced comparator. By Aptuit, Inc.