| Available : All Days | Presented By : David Nettleton |
| Category : Pharmaceutical | Event Type : Recorded Webinar |
For group or any booking support, contact: cs@conferenceschedulers.com +1 (844) 449-0244 (US Toll Free)
This webinar addresses the Computer Software Assurance guidance related to 21 CFR Part 11, and the European equivalent Annex 11 for local, and SaaS/Cloud hosted applications. It details the evolution of industry practices that increase productivity and ensure compliance. Learn the latest validation models and fill-in-the-blank templates.
Learning Objectives:
Areas Covered in the Webinar:
Who Will Benefit:
Computer System Validation’s principal, David Nettleton, is an industry leader, author, and teacher for 21 CFR Part 11, Annex 11, HIPAA, EU General Data Protection Regulation (GDPR), software validation, and computer system validation. He is involved with developing, purchasing, installing, operating, and maintaining computerized systems used in FDA-compliant applications. He has completed more than 300 mission-critical laboratory, clinical, and manufacturing software implementation projects. His most recent book is Software as a Service (SaaS) Risk-Based Validation With Time-Saving Templates, which provides fill-in-the-blank templates for completing a COTS software validation project.
| Title | Category | Type |
|---|---|---|
| Data Integrity and Privacy - compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR | Pharmaceutical | Recorded Webinar |
| Data Integrity and Privacy: Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR | Pharmaceutical | Recorded Webinar |
| Excel Spreadsheets; Ensuring Data Integrity and 21 CFR Part 11 Compliance | Pharmaceutical | Recorded Webinar |
| The 6 Most Common Problems in FDA Software Validation and Verification | Pharmaceutical | Recorded Webinar |