CPHI Milan newsletter
PCI High Potent Manufacturing
LB Bohle – 10.06.2025
Temax_Krautz

Current Edition

Current Edition

CDMO Subsection

Insights into the latest developments in CDMO services and manufacturing.

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Injectables Subsection

Expert perspectives on the evolving needs of injectable therapies and packaging.

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Nasal & Pulmonary Subsection

Exploring the latest developments in inhalation technologies, respiratory delivery and sustainability

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CPHI Milan
DDL 2026

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Nipro August 26

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Merxin March 2026

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Lifecore Biomedical

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Solstice
Product Quality Come First

Comparison of Good Manufacturing Practice Compliance Requirements – European Union, United States and India

The intentions of the current study are to expedite the compliance requirements to support the regulatory approval for selected pharmaceuticals in the United States, the European Union and India. The literature search is done using different resources like regulatory authority websites, pharmaceutical review articles, journals and public domain. To ensure the quality, all pharmaceutical manufacturers are required to establish and implement effective quality management systems. B. Naga Vamsi, Balamuralidhara V., Shenaz Z Khaleeli and Srinath S from JSS College of Pharmacy compare the GMP compliance requirements in Europe, the US and India.

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MedPharm 16/07

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Biopharma group march 2026

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Silgan March 2026

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Terumo 06/26

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Scott Pharma – 25.03.2025

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Bespak

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Tjoapack
Aptar – 08/01/2026