21 CFR Part 11 and EU Annex 11; what you need to know to pass the new Regul
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21 CFR Part 11 and EU Annex 11; what you need to know to pass the new Regul

Get ready to learn all about the latest regulations for electronic records and signatures in the US and EU - don't miss out!

Date and time

Location

Online

Refund Policy

Refunds up to 7 days before event

About this event

  • Event lasts 1 hour

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.

Webinar Takeaways

  • 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

Agenda

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
  • Data Privacy Statement
  • End

Who Will Benefit

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

Organized by

$199Jul 17 · 1:00 PM PDT