Data Integrity: Compliance with 21 CFR Part 11, SaaS-Cloud, EU GDPR

Event Details

  • DateWed 09 October 2019
  • Time10:00 AM - 11:30 AM
  • VenueOnline
  • Location39658 Mission Boulevard, Fremont National 9453
  • TypeWorkshop
  • Ticket$$150 per person
  • Table$Price for a table per table (seats Normally between 8-12)
  • ContactNetzealous LLC DBA - Compliance4all
    8004479407
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Overview: This webinar describes exactly what is required for compliance with Part 11 and the European equivalent Annex 11 for local, SaaS/Cloud hosted applications. It explains how to write a Data Privacy Statement for compliance with EU General Data Protection Regulation (GDPR). What the regulations mean is described for all four primary compliance areas: SOPs, software features, infrastructure qualification, and validation. It gets you on the right track for using electronic records and signatures to greatly increase productivity and ensure compliance. Areas Covered in the Session: What 21 CFR Part 11 means today Purpose of Part 11 What does Part 11 mean? SOPs System features Infrastructure qualification Validation Security standards Roles Usernames and passwords Restrictions and logs Data transfer standards Deleting data Encryption Audit trail standards Types of data High risk systems Electronic approval standards Electronic signatures Single sign-on Replacing paper with electronic forms Infrastructure qualification How to efficiently document qualifications Validation Software validation for vendors Computer system validation for users Fill-in-the-blank templates Change control re-validation SaaS/Cloud hosting Responsibilities for software vendor and hosting provider Evaluation criteria Hosting requirements SOPs IT, QA, validation Software development Annex 11 Comparison with Part 11 Learning Objectives: Which data and systems are subject to Part 11 and Annex 11 How to write a Data Privacy Statement What the regulations mean, not just what they say Avoid 483 and Warning Letters Requirements for local, SaaS, and cloud hosting Understand the current industry standard software features for security, data transfer, audit trails, and electronic signatures How to use electronic signatures, ensure data integrity, and protect intellectual property SOPs required for the IT infrastructure Product features to look for when purchasing COTS software Reduce validation resources by using easy to understand fill-in-the-blank validation documents Who Will Benefit: GMP, GCP, GLP, Regulatory Professionals QA/QC IT Auditors Managers and Directors Software Vendors, Hosting Providers Speaker Profile David Nettleton, is an FDA Compliance Specialist for 21 CFR Part 11, HIPAA, and Computer System Validation. His latest book is "Risk Based Software Validation - Ten easy Steps" that relates to the development, purchase, installation, operation and maintenance of computerized systems used in regulated applications.