Why You Should Consider Outsourcing Your Cloud Vendor Qualification White paper on Why You Should Consider Outsourcing Your Cloud Vendor Qualification. Various Authors - February 15, 2022 White Papers Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Quality Assurance, Regulatory
Your IT Roadmap – Guidance for Early-Stage Life Sciences Startups Learn how to create a strategic IT roadmap for early-stage life sciences companies. Address functional needs, GxP compliance, and adapt to evolving demands. Webinars Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Research & Development
Oracle Clinical One: Next Generation Clinical Trials with Continuous GxP Compliance On-demand webinar topic: Oracle Clinical One: Next Generation Clinical Trials with Continuous GxP Compliance. Webinars Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Regulatory
Computer Software Assurance (CSA) Guidance Explore the FDA's CSA guidance for risk-based computer software assurance in life sciences. Enhance compliance, product quality, and patient safety. Sandy Hedberg - February 3, 2022 White Papers Biotech, Medical Device, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory
Rapid Deployment of Enterprise-Wide GxP Applications Case study on Rapid Deployment of Enterprise-Wide GxP Applications. Erin Christy - January 18, 2022 Case Studies Biotech Clinical
EU MDR Date of Application Readiness Guide White paper on EU MDR Date of Application Readiness Guide. Jay Crowley - January 17, 2022 White Papers Medical Device Clinical, Manufacturing, Quality Assurance, Regulatory, Research & Development, Safety
