verifies that medical devices comply with applicable regulatory, safety, and quality requirements. It assesses product performance, risk management, manufacturing controls, and quality management systems
ensure that equipment, facilities, and controlled environments are properly installed, qualified, and maintained under defined conditions.
evaluates how pharmaceutical products maintain their quality, safety, and efficacy over time under defined environmental conditions.
evaluates the integrity, safety, and performance of packaging systems used for medicines. It ensures protection against contamination, moisture, light, and physical damage, while verifying compatibility with the product, seal integrity,