DATA INTEGRITY AND PRIVACY – COMPLIANCE WITH 21 CFR PART 11, SAAS/CLOUD, EU GDPR (Recorded Event )

Posted By : User Ref No: WURUR70282 0
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  • TypeWebinar
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  • Location Dufferin, Ontario, Canada
  • Price
  • Date 08-12-2020 - 08-12-2021
DATA INTEGRITY AND PRIVACY – COMPLIANCE WITH 21 CFR PART 11, SAAS/CLOUD, EU GDPR (Recorded Event ), Dufferin, Ontario, Canada
Webinar Title
DATA INTEGRITY AND PRIVACY – COMPLIANCE WITH 21 CFR PART 11, SAAS/CLOUD, EU GDPR (Recorded Event )
Event Type
Webinar
Webinar Date
08-12-2020 to 08-12-2021
Last Date for Applying
07-12-2021
Location
Dufferin, Ontario, Canada
Organization Name / Organize By
Eventura World
Presented By
David Nettleton
Sponsored By
Eventura World
Organizing/Related Departments
Training Department
Organization Type
Training/Development
WebinarCategory
Both (Technical & Non Technical)
WebinarLevel
All (State/Province/Region, National & International)
Related Industries

Education/Teaching/Training/Development

Research/Science

Biotechnology

Manufacturing

Location
Dufferin, Ontario, Canada

Description

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.

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 Should Attend:

 

  • GMP, GCP, GLP, regulatory professionals
  • QA/QC Departments
  • IT Departments
  • Auditors
  • Managers and directors
  • Software vendors, hosting providers

Areas Covered in the Session :

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

12. EU GDPR

  • Data Privacy Statement
Registration Fees
Available
Registration Fees Details
Recording - Single $350.00 Recording - Corporate $1400.00
Registration Ways
Email
Phone
Website
Address/Venue
  Recorded Event 
Official Email ID
Contact
Komala

5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada

[email protected]

     +1-416-915-4458