21 CFR Part 11 Data Integrity Training for SaaS/Cloud, EU GDPR - How to Reduce costs for compliance
2-Day Virtual Seminar
Time (Eastern Time US): 12 PM to 5 PM
Time (Central Europe): 6 PM to 11 PM
Duration: 2 DAYS
Course Director: DAVID NETTLETON
As Various parts of the world are still battling the Coronavirus (COVID-19), we are conducting the class 100% online.
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COURSE DIRECTOR
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, 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. His most 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.
Seminar Description
ABOUT THE COURSE
- This highly interactive two-day course uses real life examples and explores proven techniques for reducing costs, usually by two-thirds, associated with implementing, and maintaining computer systems in regulated environments.
- It details the requirements for Part 11 and Annex 11: SOPs, software product features, infrastructure qualification, and validation.
- The instructor addresses the latest computer system industry standards for data security, data transfer, audit trails, electronic records and signatures, software validation, and computer system validation.
- Understand the specific requirements associated with local and SaaS/cloud hosting solutions.
- Nearly every computerized system used in laboratory, clinical, manufacturing settings and in the quality process has to be validated. Participants learn how to decrease software implementation times and lower costs using a 10-step risk-based approach to computer system validation.
- The instructor reviews recent FDA inspection trends and discusses how to streamline document authoring, revision, review, and approval.
- Participants will learn how to write a Data Privacy Statement to comply with the EU General Data Protection Regulation (GDPR).
- This course benefits anyone that uses computer systems to perform their job functions and is ideal for professionals working in the health care, clinical trial, biopharmaceutical, and medical device sectors. It is essential for software vendors, auditors, and quality staff involved in GxP applications.
SEMINAR OBJECTIVES
- Reduce costs, usually by two-thirds, for compliance with electronic records
- Learn how to use electronic records and electronic signatures to maximize productivity
- Understand what is expected in Part 11 and Annex 11 inspections so you are prepared
- Avoid 483 and Warning Letters
- Understand the responsibilities and specific duties of your staff including IT and QA
- Understand your responsibilities and liabilities when using SaaS/cloud
- Learn how to perform risk-based Computer System Validation using fill-in-the-blank templates
- How to select resources and manage validation projects
- "Right size" change control methods that allows quick and safe system evolution
- Minimize validation documentation to reduce costs without increasing regulatory or business risk
- Learn how to reduce testing time and write test cases that trace to elements of risk management
- Learn how to comply with the requirements for data privacy
- Learn how to buy COTS software and qualify vendors
- Protect intellectual property and keep electronic records safe
WHO SHOULD ATTEND
- GMP, GCP, GLP, regulatory professionals
- QA/QC Departments
- IT Departments
- Engineering Departments
- Validation Departments
- Documentation Departments
- Manufacturing Departments
- Production Departments
- Operations Departments
- Auditors Departments
- Managers and directors Departments
- Software vendors, hosting providers
Agenda
- How the regulations help your company to be successful
- Which data and systems are subject to Part 11
- What Part 11 means to you, not just what it says in the regulations
Avoid 483 and Warning Letters
- Explore the four primary areas of Part 11 compliance: SOPs, software product features, infrastructure qualification, and validation documentation
- How SaaS/cloud computing changes qualification and validation
- Ensure data integrity, security, and protect intellectual property
- Understand the current computer system industry standards for security, data transfer, and audit trails
- Electronic signatures, digital pens, and biometric signatures
- 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
* Includes two 10 minute breaks and a 40 Minute Lunch break
- The Who, What, Where, When, and Why of CSV
- How to select team members
- How to facilitate a validation project
- Learn which documents the FDA expects to audit.
- How to use the risk-based validation approach to lower costs.
- How to link requirements, specifications, risk management, and testing.
- Document a computer system validation project using easy to understand fill-in-the-blank templates.
- Based on: "Risk-Based Software Validation – Ten Easy Steps" (Davis Horwood International and PDA - www.pda.org, 2006)
* Includes a 10 Minute break
- Workshop for writing requirements and then expanding them for specifications
- Step-by-step instructions for performing and documenting a risk assessment, and how to use the results to reduce validation documentation
- Reduce testing by writing test cases that trace to elements of risk management.
- How to write efficient test cases
* Includes a 40 Minute Lunch Break
- How to meet the requirements of the EU GDPR
* Includes a 10 minute break
- How to purchase COTS software and evaluate software vendors
- How to save money
- How to increase quality
- How to increase compliance with less documentation
Events
2-Day Seminar on 21 CFR Part 11 Data Integrity Training for SaaS/Cloud, EU GDPR - How to Reduce Costs for Compliance
- Date: 8/25/2022 09:00 AM
- Location Online Event
