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| home > white papers > Tightening Your Supply Chain Against Counterfeits - World Courier |
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 WHITE PAPERS |
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World Courier
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Tightening Your Supply Chain Against Counterfeits
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As today’s global pharmaceutical supply chain grows increasingly longer and more complex, each link provides added opportunity for counterfeiters.
While pending regulatory changes promise to tighten the supply chain with respect to production and distribution entities and new packaging technologies will make the identification of counterfeit products easier, the logistics of global distribution remains a weak link.
How can the pharmaceutical shipper ensure the security of the supply chain over thousands of miles and extended periods of time when the product is no longer in his possession?
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News and Press Releases |
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Northway Biotechpharma Celebrates 15 Years of Growth and Success
Vilnius, Lithuania, July 16, 2019 ─ Northway Biotechpharma, a leading
biopharmaceutical contract development and manufacturing organization
(CDMO), celebrates its 15th anniversary today. As a midsized CDMO,
Northway Biotechpharma is able to provide flexibility and responsiveness
backed by a strong foundation in science and technology. The company
focuses on understanding its customers and meeting their specific needs
without binding them to one single approach. It is able to react rapidly
to unexpected project changes, adjusting timelines, capacities and
other activities to meet its customers’ evolving needs. On average,
Northway Biotechpharma has 25–30 development projects underway each
year, ranging from gene cloning to final drug product manufacturing.
More info >> |
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White Papers |
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Device Develop for Combo Products
Phillips-Medisize
Combination products are defined as therapeutics combining two or more products (drug/device, biologics/device, biologics/drugs or drug/device/biologics), regulated and sold as a single unit. As these pharmaceutical and biological therapies and treatments have evolved, so has the need to develop appropriate delivery mechanisms for these applications. When developing a combination product, there are many things that need to be considered – the critical relationships between device development and the pharmaceutical or biologic, early establishment of regulatory and clinical strategies, understanding ‘user’ needs, determining product requirements, as well as, device manufacturing variation.
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Industry Events |
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Clinical Trials Europe | Partnerships, Outsourcing, Operations & Technology
27 August - 21 November 2019, Barcelona, Spain
On 19-21 November 2019, the clinical trial community's most influential stakeholders will be meeting in Barcelona to discuss the evolving landscape, honing in on what it takes to harness true value from partnerships, outsourcing, operations, technology and early clinical development, for a faster, more efficient route to market.
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