Instrument calibration procedure for pharmaceutical industry

Read More

• Published on: Mar 23, 2024

04 Steps to Investigate Out of Specification (OOS) Result

Read More

• Published on: Mar 08, 2024

What is cross contamination in pharmaceutical industry

Read More

• Published on: Mar 04, 2024

Good housekeeping practices in GMP

Read More

• Published on: Feb 15, 2024

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

Read More

• Published on: Dec 24, 2023

How to effectively control packaging materials in pharmaceutical

Read More

• Published on: Dec 10, 2023

SOP for surface swab test procedure for microbiology laboratory

Read More

• Published on: Nov 27, 2023

How to conduct product quality review in pharmaceutical

Read More

• Published on: Nov 19, 2023

What is meant by reference standard in Pharmaceuticals?

Read More

• Published on: Nov 06, 2023

What are the elements of quality control process in pharmaceuticals

Read More

• Published on: Oct 29, 2023

Cleaning validation protocol for pharmaceutical industry

Read More

• Published on: Sep 27, 2023

Warehouse material handling for pharmaceutical industry

Read More

• Published on: Aug 28, 2023

How to perform operational qualification – step by step

Read More

• Published on: Jul 31, 2023

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

Read More

• Published on: Jul 23, 2023

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

Read More

• Published on: Jul 14, 2023

Importance of acceptance criteria in analytical method transfer

Read More

• Published on: Jun 16, 2023

Change control management – how to implement in 06 steps?

Read More

• Published on: May 27, 2023

Data entry on quality control laboratory records

Read More

• Published on: May 05, 2023