Pharma Thread | Pharmaceutical Professionals - Page 2 of 3

Stability Studies in Pharmaceuticals: ICH Guidelines

When a patient picks up a medicine, whether it is a tablet or an injection, they trust that…

Top 10 Reasons Behind Human Errors in the Pharmaceutical Industry

In the pharmaceutical industry, every day is a challenge if the systems are operating weakly. Despite having stringent…

ready-to-use-and custom-made-endotoxin-indicators-for-depyrogenation-validation

Validating Depyrogenation Process: Meeting Ph. Eur. 5.1.12 Guidelines

In pharmaceutical manufacturing, particularly for parenteral preparations, equipment and primary packaging materials must be free from pyrogens. Pyrogens,…

terminal-sterilization-of-pharmaceutical-product

Terminal Sterilization vs. Aseptic Manufacturing

Sterile pharmaceutical products must be free from microbial contamination to ensure patient safety. The sterility of the product…

Stressed-pharma-employee-during-an-audit

Pharmaceutical Audits: How to Manage Stress During Audits?

Learn how to transform audit panic into calm confidence with proven strategies for stress management, airtight compliance, and bulletproof preparation. Because in pharma, excellence shouldn’t be a scramble—it should be your standard.

Vertical-laminar-airflow-cabinet-Pharma-thread

Laminar Airflow Cabinets and Biosafety Cabinets: Functions, Differences, and Types

Discover the key differences between laminar airflow cabinets and biosafety cabinets. Learn their types, functions, uses, and safety levels in detail.

Operator involved in equipment qualification

Pharmaceutical Equipment Qualification: From URS to Routine Usage

In any pharmaceutical industry, purchasing equipment is not just about selecting a machine and using it. It’s a systematic process that involves several steps.

Three Steps to Find a Job in the Pharmaceutical Industry as a Fresher

The pharmaceutical industry is huge and there are a lot of opportunities in this field. You need to have a systematic approach to job search.

Good Manufacturing Practices (GMP) in Pharmaceuticals

Learn about GMP in pharmaceuticals and its role in ensuring drug quality and safety. Discover the evolution to cGMP and why it’s critical for modern pharmaceutical manufacturing.

Production of Water for Injections (WFI)

Validating Depyrogenation Process: Meeting Ph. Eur. 5.1.12 Guidelines

Common Types of Documentation Errors in the Pharmaceutical Industry

Stability Studies in Pharmaceuticals: ICH Guidelines

Top 10 Reasons Behind Human Errors in the Pharmaceutical Industry

Validating Depyrogenation Process: Meeting Ph. Eur. 5.1.12 Guidelines

Terminal Sterilization vs. Aseptic Manufacturing

Pharmaceutical Audits: How to Manage Stress During Audits?

Laminar Airflow Cabinets and Biosafety Cabinets: Functions, Differences, and Types

Pharmaceutical Equipment Qualification: From URS to Routine Usage

Three Steps to Find a Job in the Pharmaceutical Industry as a Fresher

Good Manufacturing Practices (GMP) in Pharmaceuticals

Production of Water for Injections (WFI)

Risk Assessment for Environmental Monitoring in Sterile Injectable Facilities

What Is FDA 483 Observations?

Essential Microbiology Techniques in Pharmaceuticals: A Guide for Accuracy and Compliance