info@grcmeeting.com +1-661-336-9555

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

instructor
By: David Nettleton
Schedule: 20 November, 2024 (Wednesday)
Time: 10:00 AM PDT | 01:00 PM EDT
Duration: 90 Minutes
Webinar ID : 2501

    Countdown for your webinar:

  • days
  • Hrs
  • Mns
  • Secs
Currency:

Live Webinar Options

On Demand Options

Group Session Options

Live Session with unlimited participants. Invite any number of attendees to join.


Webinar Details

This webinar describes exactly what is required for compliance with Computer Software Assurance guidance, 21 CFR Part 11, and the European equivalent Annex 11 for local, and 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.

AREA COVERED

  • 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
  • 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
  • GMP, GCP, GLP, Regulatory Professionals
  • QA/QC
  • IT
  • Auditors
  • Managers and Directors
  • Software vendors, Hosting Providers

SPEAKER PROFILE

instructor

Computer System Validation’s principal, David Nettleton is an industry leader, author, and teacher for 21 CFR Part 11, Annex 11, HIPAA, EU GDPR software validation, and computer system validation. He is involved with the development, purchase, installation, operation, and maintenance of 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.

Upcoming Webinars