EU MDR Date of Application Readiness Guide White paper on EU MDR Date of Application Readiness Guide. 0 Jay Crowley - January 17, 2022 White Papers Medical Device Clinical, Manufacturing, Quality Assurance, Regulatory, Research & Development, Safety
Is it Acceptable to Push Back if You Disagree with a Notice of Violation or 483? Blog article topic: Is it Acceptable to Push Back if You Disagree with a Notice of Violation or 483? 0 Diane Gleinser - January 13, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory, Safety
Benefits of Pharmaceutical Serialization Blog article topic: Benefits of Pharmaceutical Serialization. 0 Jim Macdonell - January 9, 2022 Blogs Pharma Regulatory, Safety
2022 Trends in Life Sciences White paper on 2022 Trends in Life Sciences. 0 Various Authors - November 4, 2021 White Papers Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory, Research & Development, Safety
The Direct Marking of Medical Devices in the U.S. and Europe White paper on The Direct Marking of Medical Devices in the U.S. and Europe. 0 Jay Crowley - April 18, 2021 White Papers Medical Device Information Technology, Manufacturing, Quality Assurance, Regulatory, Research & Development, Safety
On-site and Remote Audit Best Practices Blog article topic: On-site and Remote Audit Best Practices. 0 Vega Finucan - March 7, 2021 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory, Safety
