by Naveen kumar | Oct 10, 2024
Unveiling the Role of the Analytical Quality Assurance (AQA) Department in Pharma In the world of pharmaceuticals, quality is everything. That’s where the Analytical Quality Assurance (AQA) department steps in, ensuring that every drug produced meets strict...
by Naveen kumar | Sep 24, 2024
HVAC Systems in Pharmaceuticals: Ensuring Optimal Conditions for Quality Production Heating, Ventilation, and Air Conditioning (HVAC) systems are critical components in pharmaceutical manufacturing, ensuring the proper environmental conditions necessary for the...
by Naveen kumar | Sep 9, 2024
GMP vs. cGMP in Pharma: What’s the Difference? In the pharmaceutical world, making safe and high-quality medicines is essential. That’s where GMP (Good Manufacturing Practices) and cGMP (Current Good Manufacturing Practices) come in. While they sound similar, they...
by Naveen kumar | Aug 28, 2024
Why Magnetic rods are used in Cleaning Verification in Pharma If you see, some regulatory agencies keep strict limits on metal contamination in pharmaceutical products. This is a very good initiative as it improves the quality of the medicines we consume. Prevention...
by Naveen kumar | Aug 13, 2024
“Understanding Master Copy, Control Copy, and Obsolete Copy in the Pharmaceutical Industry” In the Pharmaceutical industry document issue is very important and every document is traceable and accountable in the form of master copy, control copy, and...
