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The US Food and Drug Administration (FDA) has made the decision to delay the active enforcement of the Drug Supply Chain Security Act (DSCSA), aimed at combatting the issue of counterfeit medicines entering the supply chain.

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With the deadline for new regulations on serialisation looming closer for both the US and European markets, the biggest challenge many pharmaceutical companies face is time.

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Oncopeptides have collaborated with Recipharm to help bring their anti-cancer treatment to life.

Oncopeptides is a clinical stage company that is developing a molecule for oncologyindications. The molecule, which originated at Uppsala University, Sweden and the Karolinska Institute, is focused on multiple myeloma as a first indication.

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Serialisation represents a significant challenge for CDMOs, with multiple factors to consider, from varying market regulations to data storage and exchange.  

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With US serialisation requirements about to come into force and EU regulations on the horizon, more and more businesses are considering what track and trace could mean for them beyond compliance.

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ABSTRACT: Aminopeptidases like aminopeptidase N (APN, also known as CD13) play an important role not only in normal cellular functioning but also in the development of cancer, including processes like tumor cell invasion, differentiation, proliferation, apoptosis, motility, and angiogenesis.

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Demand for outsourced contract manufacturing in the pharmaceutical industry continues to grow, but what does it take to be a trusted partner?

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The current pharmaceutical industry landscape creates some interesting opportunities for CDMOs to grow and develop.

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In the last ten years, the contract manufacturing sector has experienced some major changes as a result of consolidation, increasing price pressures and evolving customer expectations.

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Amjad Alhalaweh, one of our formulation scientists at Recipharm, took part in the in-Pharma Technologist Drug Delivery online conference on Thursday 20th April, 2017.