Rework procedure in pharmaceutical manufacturing – Step-by-step guide

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• Published on: Mar 06, 2025

How to develop GMP compliant software for quality management

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• Published on: Jan 29, 2025

Chemical spill response, step-by-step procedure for pharmaceutical operations

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• Published on: Dec 06, 2024

Stability testing best practice for Pharmaceutical products

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• Published on: Nov 15, 2024

How to ensure quality and compliance in clinical supply chain management

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• Published on: Aug 11, 2024

Quality planning best practice for medical device and GMP

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• Published on: Jul 15, 2024

Deviation investigation guidelines in the pharmaceutical industry

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• Published on: Jun 28, 2024

Overview of pharmaceutical quality control steps and implementations

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• Published on: Jun 10, 2024

What is analytical laboratory management in pharmaceutical?

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• Published on: Jun 06, 2024

Validation master plan (VMP) – when and how to create one?

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• Published on: Jun 01, 2024

GMP cleaning and sanitation practices in pharmaceuticals

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• Published on: May 18, 2024

Concept of process validation in pharmaceutical industry

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• Published on: Apr 25, 2024

Guideline for Excel spreadsheet validation

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• Published on: Apr 19, 2024

GMP rules to keep pharmaceutical warehouse in perfect condition

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• Published on: Apr 03, 2024

Line clearance procedure and reconciliation in GMP

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• Published on: Mar 30, 2024

What is computer system validation (CSV) in GMP

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• Published on: Mar 25, 2024

Instrument calibration procedure for pharmaceutical industry

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• Published on: Mar 23, 2024

04 Steps to Investigate Out of Specification (OOS) Result

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• Published on: Mar 08, 2024