USFDA Audit Process in Pharmaceuticals
The USFDA audit process, also referred to as an FDA inspection, is a structured, risk-based, on-site examination…
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January 30, 2026
Calibration in Pharmaceuticals
Calibration in pharmaceuticals is one of the most fundamental activities in the industry. Every measurement we record—temperature,…
January 29, 2026
Step-by-Step Guide to Setting Up a Pharmaceutical Cleanroom
Setting up a pharmaceutical cleanroom is one of the most critical activities in the pharmaceutical industry. A…
January 28, 2026
Disinfectants in Pharmaceutical Cleanrooms: Types, Uses, and Best Practices
Introduction Disinfectants in pharmaceutical cleanrooms play a vital role in controlling microbial contamination and ensuring that medicines…
January 28, 2026
ALCOA Principles in Pharmaceuticals
ALCOA principles are the foundation of data integrity in the pharmaceutical industry. Every test result, record, and…
January 27, 2026
Adverse Effects in Clinical Trials: ICH Guidelines
Adverse effects in clinical trials are not just for clinical research teams. They are relevant to everyone…
January 7, 2026
Microorganisms of Concern vs Objectionable Microorganisms in Pharmaceuticals
One topic that often creates confusion among freshers and even experienced professionals is microorganisms of concern vs…
January 3, 2026