Introduction Current Good Manufacturing Practices (cGMP) represent the guidelines enforced by regulatory agencies such as the U.S. Food and Drug Administration (FDA) to ensure that pharmaceutical products are consistently produced and controlled according to quality...
Humidity is a crucial environmental parameter in many industrial, commercial, and residential applications. Accurate humidity measurements are vital for various processes, such as pharmaceuticals, food production, agriculture, and HVAC systems. However, over time, humidity sensors can drift and produce inaccurate readings due to wear, exposure to contaminants, or harsh environmental conditions. Therefore, regular calibration of humidity instruments is essential to ensure their accuracy and reliability.
In the pharmaceutical, biotech, and medical device industries, ensuring the stability of products is a critical aspect of quality control. Stability chambers are essential tools used for testing how products react under different environmental conditions over time,...
Introduction ISO 9001:2015 is one of the most recognized international standards for quality management systems (QMS). It sets out the criteria for a QMS and is based on several quality management principles, including a strong customer focus, process-based...
Introduction Calibration is a critical process in the pharmaceutical industry, ensuring that instruments used in drug production and testing perform accurately and reliably. The role of calibration extends beyond merely maintaining the functionality of equipment—it...
Pharmaceutical manufacturers must have a calibration program for their equipment to ensure the accuracy and precision of measurements that directly impact the quality, safety, and efficacy of their products.