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• 21 CFR Part 11: An FDA Regulatory Compliance for Electronic Records

  Since 1997, hospitals, pharmaceutical companies and other regulated businesses have moved record keeping, retrieval and storage from paper to electronic systems at a rapid rate. The shift was driven largely by faster and safer data exchange around the world. Title 21 CFR Part 11, the FDA regulation on electronic records …

• Medical Device Compliance: Key ISO, MDSAP and EU MDR Updates

  Medical devices sit at the top of the compliance list in healthcare, because the rules that govern them change often and the stakes are high. Devices save lives, so every organization that makes or supplies them has to make sure they are safe and sterile. This article explains the main …

Related Blogs

21 CFR Part 11: An FDA Regulatory Compliance for Electronic Records

Medical Device Compliance: Key ISO, MDSAP and EU MDR Updates

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