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The impact of particles on pharmaceuticals

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The impact of particles on pharmaceuticals

Sometimes it's the smallest details that have the biggest impact on pharmaceutical performance. That's certainly true when it comes down to the properties of particles and their impact on pharmaceutical performance. Subtle changes in particle...

The role of dissolution in drug development

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The role of dissolution in drug development

Oral dosage forms remain one of the most flexible and effective treatments available to patients. Dissolution testing is a requirement for all solid oral dosage forms and is used throughout the development life-cycle for product release and stability...

Method development – why it matters to get it right

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Method development – why it matters to get it right

In an industry that is seeing increasing levels of outsourcing, the contract research organisation (CRO) needs to have proven experience in both the pragmatism and flexibility of method development and a regulatory background in validation.

Impurity isolation and sample purification

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Impurity isolation and sample purification

During a manufacturing process unexpected and unknown impurities may arise in a sample. It is important that such impurities are isolated and identified.

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Take steps to stay in the serialization race

As the deadline for drug serialization in the EU looms closer, it’s time to put the topic firmly on your agenda. Learn how to overcome the serialization challenge and simplify compliance.

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