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ABB India bags order to automate Reliance Life Sciences’ biopharma facilities

Express Pharma

The company did not disclose the value of the order ABB India on Monday announced that it has secured a major automation contract from Reliance Life Sciences (RLS) to automate its manufacturing plants in Nashik. Large-scale biotechnology production presents distinct and complex process and automation challenges.

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Alternative methods for mycobacterial testing in biological products

European Pharmaceutical Review

Following a review on the suitability of different technologies, researchers have determined that “[nucleic acid amplification techniques] NATs combined with an efficient extraction method” is the fitting alternative for compendial mycobacterial testing in biological products. A further limitation, Marius et al.

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QA/QC & Microbiology In-Depth Focus 2023

European Pharmaceutical Review

She discusses rapid sterility testing methods, regulatory frameworks, and the impact of automation and digitalisation on microbiological quality control. The post QA/QC & Microbiology In-Depth Focus 2023 appeared first on European Pharmaceutical Review.

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BMS to boost CAR T cell therapy production with Cellares deal

Pharmaceutical Business Review

Under the terms of the agreement, Cellares will streamline, automate, and transfer technology for selected BMS CAR T cell therapies onto its Cell Shuttle manufacturing platform. Additionally, BMS joined the Cellares Technology Adoption Partnership (TAP) programme to analyse the automated manufacturing expertise of Cell Shuttle.

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Control strategy could facilitate faster bioburden detection

European Pharmaceutical Review

Biopharma and bioprocessing experts have proposed an approach that uses a two-tiered control strategy for rapid bioburden testing, that can beneficially, “leverage faster detection times”. Specifically, the first assay is “suited for continuous in-process demonstration of the validated state”.

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The role of GAMP 5, data integrity and QbD in pharmaceutical quality assurance

European Pharmaceutical Review

The authors explained first that “a robust quality assurance framework” is needed to ensure medicinal products are safe and efficient. defined GAMP as ‘good automated manufacturing practices’, with GAMP 5 being “a widely used framework for validating automated systems that establishes quality assurance practices. Pedro et al.

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Cadila Pharma launches API manufacturing plant at Dahej

Express Pharma

Equipped with Distributed Control System (DCS) automation technology, the facility has been set up with an investment of Rs 200 crore Cadila Pharmaceuticals inaugurated its state-of-the-art Active Pharmaceutical Ingredients (API) Plant at Dahej in the Bharuch district. Koshia, Food Drug Commissioner for Gujarat, and Dr M.

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