Pharmaceutical sampling procedures for non-sterile products

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• Published on: Feb 25, 2023

What is environmental monitoring in pharmaceutical industry

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• Published on: Dec 29, 2022

Basic Overview of Contamination Control in GMP Facility

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• Published on: Oct 16, 2022

How to implement good documentation practice in a GMP regulated plant

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• Published on: Oct 16, 2022

What is acceptable quality limit and how to use AQL in sampling

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• Published on: Sep 22, 2022

How to use quality risk management in validation testing

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• Published on: Aug 23, 2022

Six steps procedure for corrective and preventive action

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• Published on: May 15, 2022

How to conduct GMP training for employee

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• Published on: Apr 28, 2022

Seven steps to complete a supplier selection process in GMP

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• Published on: Apr 12, 2022

How to conduct a root cause investigation using DMAIC principle

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• Published on: Mar 29, 2022

How to develop supplier relationship management strategies in GMP

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• Published on: Mar 11, 2022

Basic understanding of quality assurance in GMP

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• Published on: Feb 06, 2022

How to perform metal detection in pharmaceuticals processes

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• Published on: Feb 03, 2022

How to test, adjust and balance HVAC systems

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• Published on: Nov 28, 2021

How to perform periodic review of systems and processes in pharmaceuticals?

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• Published on: Nov 10, 2021

Better Understanding of International GMP Regulatory Requirements

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• Published on: Oct 06, 2021

Quality Agreements with Third Party Manufacturer

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• Published on: Sep 03, 2021

Computer system electronic record standard

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• Published on: Jul 08, 2021