Quality Control
A business request?
Quality Control (QC) is an essential process that ensures products meet the required safety, efficacy, and quality standards before they reach the market.
This involves rigorous testing and evaluation of pharmaceuticals, biotechnology products, and medical devices at various stages of production to identify and rectify any defects or deviations from the established standards.
Quality Control procedures are critical in maintaining the integrity of the production process, from raw material inspection to the final product release, ensuring that every item complies with regulatory requirements and meets the industry’s high standards of quality and reliability. Through these meticulous QC processes, companies in the Life Sciences sector can guarantee that their products are consistently safe and effective for consumer use, ultimately safeguarding public health.
“Quality Control’s final goal is to make sure that testing is performed following regulations and international standards. Some acceptance criteria must be met, specific analysis have to be done, and data recorded following integrity principles. Overall, we need to ensure that products meet the standards of safety, efficacy, and purity, to improve patient’s lives.“
Michele Malandruccolo
