PharmiWeb.com - Global Pharma News & Resources
23-May-2019 - 23-May-2019

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

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.

Why should you attend this webinar?

Our Speaker David Nettleton will explain: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


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 11End
    • Comparison with Part 11
  • End

Who can Benefit:

  • GMP, GCP, GLP, regulatory professionals
  • QA/QC
  • IT
  • Auditors
  • Managers and directors
  • Software vendors, hosting providers
  • Industries:
  • Pharmaceutical
  • Medical device
  • Biologic
  • Food
  • Cosmetics
  • FDA Regulated Companies
  • Software Vendors
  • SaaS providers
  • Data centers

Industries:

  • Pharmaceutical
  • Medical device
  • Biologic
  • Food
  • Cosmetics
  • FDA Regulated Companies
  • Software Vendors
  • SaaS providers
  • Data centers

 

Speaker Profile:

David Nettleton is a keynote speaker of ComplianceKey. 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, installation, operation, and maintenance of computerized systems used in FDA compliant applications. He has completed more than 280 mission critical laboratory, clinical, and manufacturing software implementation projects. His most popular book is Risk Based Software Validation - Ten Easy Steps, which provides fill-n-the-blank templates for completing a COTS software validation project.

Register: https://www.compliancekey.us/webinarDetails?industryId=3&webinarid=1385&speakerid=249

Contact Info:

Compliance Key

Email: support@compliancekey.us

Visit: https://www.compliancekey.us/upcoming-webinar

Phone: +1 717-208-8666