Good laboratory practice (GLP) regulations – FDA requirements for laboratoriess

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• Published on: Dec 24, 2023

How to effectively control packaging materials in pharmaceutical

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• Published on: Dec 10, 2023

SOP for surface swab test procedure for microbiology laboratory

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• Published on: Nov 27, 2023

How to conduct product quality review in pharmaceutical

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• Published on: Nov 19, 2023

What is meant by reference standard in Pharmaceuticals?

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• Published on: Nov 06, 2023

What are the elements of quality control process in pharmaceuticals

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• Published on: Oct 29, 2023

Cleaning validation protocol for pharmaceutical industry

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• Published on: Sep 27, 2023

Warehouse material handling for pharmaceutical industry

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• Published on: Aug 28, 2023

How to perform operational qualification – step by step

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• Published on: Jul 31, 2023

A step-by-step guide to successful installation qualification (IQ)

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• Published on: Jul 23, 2023

Equipment cleaning procedure (SOP) in pharmaceutical, Do’s and Don’ts

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• Published on: Jul 14, 2023

Importance of acceptance criteria in analytical method transfer

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• Published on: Jun 16, 2023

Change control management – how to implement in 06 steps?

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• Published on: May 27, 2023

Data entry on quality control laboratory records

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• Published on: May 05, 2023

How to prepare for a GMP warehouse audit – tips and tricks

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• Published on: Apr 29, 2023

Typical GMP documentation in a quality control laboratory

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• Published on: Apr 03, 2023

Corrective and Preventive Action (CAPA) Procedure for GMP

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• Published on: Mar 18, 2023

What is quality risk management in pharmaceutical?

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• Published on: Mar 05, 2023