Bookmark Add to Calendar

Data Integrity and Privacy: Compliance with 21 CFR Part 11 and Annex 11

Duration : 90 Minutes

David Nettleton,

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 the development, purchase, installati Read more

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.

Course 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

Course Outline:

1. What 21 CFR Part 11 means today 

• Purpose of Part 11

2. What does Part 11 mean?

• SOPs

• System features

• Infrastructure qualification

• Validation

3. Security standards

• Roles

• Usernames and passwords

• Restrictions and logs

4. Data transfer standards

• Deleting data

• Encryption

5. Audit trail standards

• Types of data

• High risk systems

6. Electronic approval standards

• Electronic signatures

• Single sign-on

• Replacing paper with electronic forms

7. Infrastructure qualification

• How to efficiently document qualifications

8. Validation

• Software validation for vendors

• Computer system validation for users

• Fill-in-the-blank templates

• Change control re-validation

9. SaaS/Cloud hosting

• Responsibilities for software vendor and hosting provider

• Evaluation criteria

• Hosting requirements

10. SOPs

• IT, QA, validation

• Software development

11. Annex 11

• Comparison with Part 11


• Data Privacy Statement

What You Get:

• Training Materials

• Live Q&A Session with our Expert

• Participation Certificate

• Access to Signup Community (Optional)

• Reward Points

Who Will Benefit:

• GMP, GCP, GLP, regulatory professionals


• IT Personnel

• Auditors

• Managers and Directors

• Software vendors, Hosting providers

Please reach us at 1-888-844-8963 for any further assistance or if you wish to register

Contact Us

Similar Trainings

Advanced Auditing Strategies for Data Integrity Risks
LIVE : Scheduled on 01-February-2023 :03:00 PM EST
Human Factors-Usability Based on ISO 62366
LIVE : Scheduled on 02-February-2023 :01:00 PM EST
How to Prepare a 510(k) Submission
LIVE : Scheduled on 03-February-2023 :01:00 PM EST
21 CFR 58 - Good Laboratory Practice (GLP) and USP 1058 Validations
LIVE : Scheduled on 07-February-2023 :01:00 PM EST
Write it Right – Well Written Procedures are Essential for QMS Effectiveness
LIVE : Scheduled on 15-February-2023 :01:00 PM EST
paypal payment Comodo

Copyright ©2023 All rights reserved. | DBA