Data integrity is established where the data is stored and managed in its original form. Discover why the FDA expects manufacturers to ensure all data meets the guidelines outlined in the ALCOA acronym.
Explore the urgent need for businesses to adopt strong data integrity practices and identifies measures for how to achieve and sustain compliance.
A CAPA management system can provide your company with the ability to recognize and correct risks. Learn how to ensure your CAPA management system benefits the manufacturing process.
Learn how to embed risk-based thinking into quality efforts with an integrated risk management software.
Six steps to reducing the time, pain, and expense of the software validation process while maintaining quality and safety.
Learn how to improve traditional risk management methods and tools and how AI can help in the identification and mitigation of risk.
Learn how a modern Manufacturing Execution System (MES) is using digital production records to help manufacturers regulated by the FDA improve their quality and efficiency goals.
What requirements should cell and gene therapy developers meet to successfully bring innovative therapies to market?
Learn how digital solutions and a modern ERP system can effectively combat counterfeit med devices and pharmaceuticals to improve patient safety and business performance.
QSR compliance can be complex, but it doesn’t have to be burdensome. Implementing these best practices will improve your regulatory compliance while producing a product ready for market.
Get the latest articles from Pharmaceutical Online delivered to your inbox.