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Asahi Kasei Bioprocess and Axolabs partner to accelerate oligonucleotide therapeutics development

Express Pharma

By selectively manipulating specific molecular processes, these therapies hold the potential to treat a wide range of diseases (e.g., This cooperation aims to accelerate the development and commercialisation of oligonucleotide-based therapies to improve quality of life for patients worldwide.

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Biologics driving continuous bioprocessing market expansion

European Pharmaceutical Review

With a wider focus on sustainability in the industry, continuous bioprocessing aligns with these goals due to its ability to require less resources when compared to batch processing, the research stated. As such “establishing regulatory acceptance and compliance for continuous processes can be a significant challenge”.

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Single-use bioprocessing market to value $84.14bn by 2032

European Pharmaceutical Review

Yet the single-use bioprocessing market face several challenges, such as concerns about the quality and consistency of single-use products, the lack of standardisation in the industry, supply chain security and the high cost of single-use equipment. Could centrifugal bioreactor accelerate cell-therapy manufacturing?

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Overcoming the Challenges of Drug Development in a CDMO setting

PharmaTech

Responding to the development of more novel therapies and fast-track designations means being equipped with the right processes and resources to support expedited approvals right from the beginning of process development.

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A comprehensive guide to planning, targeting, and selling medtech (and everything in between)

Definitive Healthcare

Resource Type E-Books & How-To Guides eBook eBook eBook Developing an omnichannel strategy for life sciences Artificial intelligence and machine learning for medical device companies Launching your medical device: A strategy and execution cross-functional guide Image Image Image ","nextArrow":" ","appendArrows":".coh-slider-nav-bottom","dots":false,"draggable":true,"swipe":true,"fade":false,"vertical":false,"speed":700,"cssEase":"ease","pauseOnHover":false,"pauseOnDotsHover":false,"autopl

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A step-by-step guide to successful installation qualification (IQ)

GMPSOP

In summary, the intent of installation qualification is to produce evidence that the equipment has been built and installed in compliance with their design specifications. Furthermore, the installation qualification test creates evidence that all the primary features of the equipment are available as designed.

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Elevating pharmaceutical manufacturing processes with real-time insights

European Pharmaceutical Review

To address these issues, companies should adopt more advanced production strategies such as continuous flow chemistry, as they can shorten manufacturing processes, increase productivity and throughput. As a result, PAT enhances process understanding and regulatory compliance while ensuring consistent product quality.