PCI High Potent Manufacturing
LB Bohle – 10.06.2025
Temax_Krautz

Current Edition

Current Edition

Subsection - CDMO

Examining how innovative technologies, integrated manufacturing approaches and AI are shaping manufacturing.

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Subsection - Injectables

Exploring advances in injectable drug delivery and sterile manufacturing, designed to improve patient-centric delivery.

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Subsection - Neurodegenerative Diseases

Exploring emerging approaches to neurodegenerative disease research and treatment.

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Subsection - Nasal & Pulmonary

Highlighting how advances in nasal and pulmonary drug delivery, formulation, devices and analytics are enabling more complex therapies.

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Lifecore Biomedical

In the Pharmaceutical GMP Industry: If Quality Is Everyone’s Responsibility, Is It No One’s Responsibility?

The phrase “Quality is everyone’s responsibility” is often misinterpreted in the Pharmaceutical Inspection Cooperation Scheme – Good Manufacturing Practices (PIC/S GMP) pharmaceutical industry, leading to the belief that quality oversight is solely the responsibility of the Quality Assurance (QA) department.

This article explores the critical role of QA professionals in fostering a collaborative quality culture, asserting that quality should be integral to every employee’s responsibility. It emphasises management commitment in establishing effective Pharmaceutical Quality System (PQS) and encourages viewing QA as partners. By engaging teams across various functions, organisations can cultivate a unified commitment to quality and implement strategies for overcoming resistance and measuring success through quantifiable metrics.

Introduction

In the regulated pharmaceutical GMP industry, the phrase “Quality is everyone’s responsibility” is often misinterpreted, leading to the belief that quality is solely the QA department’s responsibility. This disconnect can foster neglect of quality oversight, with employees feeling their roles don’t impact overall quality. This article addresses these misconceptions and highlights the vital role of QA professionals in fostering a culture of quality. It emphasises the need for management to promote quality actively and for all employees to recognise their contributions to product integrity and patient safety. By viewing quality as integral to every role, organisations can enhance their commitment to excellence and continuous improvement.

Edwards Deming famously stated, “Quality is everyone’s responsibility.”¹ While this sentiment is valid, it can easily be misinterpreted. If Deming’s quote is considered in isolation, it risks falling into the familiar “everybody, somebody, nobody” trap, where individuals assume that someone else is accountable for quality. This leads to complacency and oversight. It is important to recognise that most employees do not come to work intending to perform poorly or resist improvement. When lapses occur, it is often due to a lack of awareness or clarity regarding their responsibilities.

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Scott Pharma – 25.03.2025

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Tjoapack
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