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With FDA’s Food Safety and Modernization Act (FSMA), importers were given greater responsibility for ensuring that ...
Clinical evidence is required to assure the safety and efficacy of a medical device for intended use pre-market. ...
The Food and Drug Administration (FDA) has requirements for medical device manufacturers to establish and maintain ...
The Food Safety and Modernization Act (FSMA) was signed into law in 2011, with compliance dates for some ...
Colors can set apart your medical device, drug, food, and cosmetic. But, do you know how FDA permits their use ...
The European Medicines Agency (EMA) and the United States FDA have fully implemented the Mutual Recognition ...
ISO 14971 is the ultimate gold standard for risk management for medical devices. It was developed to provide ...
Nonconforming products happen but managing them before they spin out of control is important. With QualiPro you ...
The U.S. Food and Drug Administration is offering another opportunity for stem cell clinics to work with the ...
The $40 billion dietary supplement industry is still growing making it a market you may want to take advantage of, ...
FDA regulates the labeling and advertising of all pharmaceutical products; however, it regulates the labeling of ...
Having a good CAPA management system is a key element in making sure your CAPA process is successful. QualiPro has ...
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