One of the most widely used ISO standards in the pharmaceutical, biotechnology, and medical device industry is ISO 13485, which specifies the requirements for a quality management system for ...

New Delhi: Life-saving medical devices will soon have to face tougher safety norms. The Central Drugs and Standards Control Organization (CDSCO) and the Bureau of Indian Standards (BIS) are ...

IntroductionIn the rapidly evolving healthcare landscape, medical devices play a pivotal role in enhancing patient care and improving health outcomes. The road to getting these devices from concept to ...

Successfully integrate components like MEMS and sensors by considering every aspect of the device from the outset.

ISO 13485 is an internationally recognized standard for quality management systems, created by the International Organization for Standardization to ensure the safety and effectiveness of medical ...

Many AI-enabled medtech products leverage machine learning or deep learning. In order to address the opaque decision-making processes, explainability is essential to enhance trust, safety, and ...

Woman- and Family-Owned Medical Device Assembly and Packaging Company Marks 45 Years of Sustained GrowthSanta Fe Springs, California--(Newsfile ...