Challenges with EU MDR and IVDR Compliance On-demand webinar topic: Challenges with EU MDR and IVDR Compliance. Webinars Medical Device Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory, Safety
Cybersecurity Threats and Risks to Life Sciences Companies On-demand webinar topic: Cybersecurity Threats and Risks to Life Sciences Companies. Webinars Biotech, CMO, CRO, Medical Device, Pharma Information Technology
FDA Mandated Global CSV Remediation Case study on FDA Mandated Global CSV Remediation. Diane Gleinser - April 12, 2022 Case Studies Medical Device Information Technology, Quality Assurance, Regulatory
Validating SharePoint for Life Sciences Regulated Environments Blog article topic: Qualifying SharePoint for Life Sciences Regulated Environments. Hovsep Kirikian - April 11, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory
Content Orchestration Blog article topic: Content Orchestration. Vishal Sharma - April 11, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Quality Assurance
Global UDI Database: What if a Medical Device is Discontinued? At some point in the future when a product is no longer distributed, the medical device company will need to... Jay Crowley - April 8, 2022 Blogs Medical Device Manufacturing, Regulatory
