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As the biopharmaceutical industry gains momentum and biological products are being heavily investigated as treatment modalities, measures are needed throughout to ensure their overall safety and quality from microbiological contamination.

Contamination Control During Biopharmaceutical Processing

The changes during biopharmaceutical manufacturing, processing and storage can impact the safety and efficacy of products during clinical use. Controlling such product variability is a challenge to maintaining batch-to-batch consistency.

Maintaining Batch-to-Batch Consistency

Assuring sample integrity and security during the development, manufacturing, and supply of biopharmaceuticals is one of the most important aspects leading to establishing standards that guarantee proper sample security.

Sample Security within the Biopharmaceutical Industry

Crystallization of challenging pharmaceutical targets to aid drug discovery

Flexibility and capability in pre-filled syringes

Orphan Drug Development – A pragmatic approach to developing a rare disease drug

Prefabricated GMP Cleanrooms for Aseptic Filling

This application note demonstrated an early placement of our ‘in-house’ developed rheological test in the preformulation studies to select right type and amount of lubricant in the formulation, and, if necessary, the desired coating of punches. 


Powder Rheology: Gateway for Tablet Sticking Insights

Explore how next-gen QMS delivers digital transformation by seamlessly connecting enterprise-wide systems, processes,, documentation, and data in a cost-effective manner

Cost Effective QMS Digital Transformation

Applying Digital Solutions & QbD to Optimize Topical Product Development

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