Overview:
This webinar describes
exactly what is required for compliance with 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.
Areas covered during the
session:
- 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
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
EU GDPR
- Data Privacy Statement
- end
What industries will benefit from this training:
- Pharmaceutical
- Medical Device
- Biologics
- Food
- Cosmetics
- FDA regulated companies
- Software Vendors
- SaaS providers
- Data Centers.
Who will benefit?
- GMP, GCP, GLP, regulatory professionals
- QA/QC
- IT
- Auditors
- Managers and directors
- Software vendors, hosting
providers
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.
Mr. Nettleton 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.
Mr. Nettleton 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.