Demystify FDA Compliance for Public Cloud Workloads in Life Sciences Explore best practices for FDA-compliant cloud adoption in life sciences. Learn about workload analysis, compliance management, and secure cloud strategies. Webinars Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
Five Tips for Successful Veeva Implementation Blog article topic: Five Tips for Successful Veeva Implementation. Donald Zinn - April 14, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology
Cannabis: Compliance in a Rapidly Changing Industry On-demand webinar topic: Cannabis: Compliance in a Rapidly Changing Industry. Webinars Pharma Clinical, Manufacturing, Quality Assurance, Regulatory, Safety
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
Single Sign-on Significantly Improves Security and Usability Blog article topic: Single Sign-on Significantly Improves Security and Usability. Lisa Om - April 7, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
Master Data Management and Validation to Meet Global Requirements Case study on Master Data Management and Validation to Meet Global Requirements. Jay Crowley - April 7, 2022 Case Studies Medical Device Information Technology, Quality Assurance, Regulatory
