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Transforming pharmaceutical manufacturing: The AI revolution

European Pharmaceutical Review

Revolutionising quality control In the backdrop of stringent quality standards and regulatory demands inherent to pharmaceutical manufacturing, the addition of AI technologies introduce a paradigm shift. Integrative Analysis of Multi-Omics Data with Deep Learning: Challenges and Opportunities in Bioinformatics.

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Beyond instruments: streamlining process technology implementation in biopharmaceutical manufacturing

European Pharmaceutical Review

Implementing PAT in (bio)pharmaceutical manufacturing New sensors or larger equipment with more complex setups (software and hardware) require stringent procedures to become fully implemented in a good manufacturing practice (GMP) manufacturing facility. Good Design Practices for GMP Pharmaceutical Facilities.

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Warnings for Japanese pharmaceutical market may lead to more lenient price controls

Pharmaceutical Technology

According to the report, five member companies decided to decrease their investment in Japan between 2016 and 2017, four companies changed their investment targets between 2018 and 2020, and one company lowered the priority given to Japan after 2021.

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Warnings for Japanese pharmaceutical market may lead to more lenient price controls

Pharmaceutical Technology

According to the report, five member companies decided to decrease their investment in Japan between 2016 and 2017, four companies changed their investment targets between 2018 and 2020, and one company lowered the priority given to Japan after 2021.

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An Annex 1 and Pharma 4.0 perspective on water quality

European Pharmaceutical Review

Her current research is focused on spectroscopy and mathematical modelling as process analytical technologies in pharmaceutical manufacturing. Inspection Technical Guide – Water for Pharmaceutical Use. Chemie Ingenieur Technik , 2016, Årg. References. US Food and Drug Administration. Minnish C, Hardy S, Krämer S.

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Paradigm Shift in Drug Development: Analytical Quality by Design and Analytical Procedure Life Cycle

Quality Matters

Paradigm Shift in Drug Development: Analytical Quality by Design and Analytical Procedure Life Cycle In today’s pharmaceutical manufacturing environment, companies face increasing pressure to respond to changing demands across the global medicines supply chain while still maintaining the quality of their drug products.

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DSCSA

Ramblings of a pharmacist

files in order to comply with the EDDS requirements, but the fact that we’ve now known since at least 2016 that EPCIS would be the way that the EDDS data transfer requirements would be executed by McKesson, it’s rather disappointing that a company with $284 billion in revenue is still using.856