Dublin, Oct. 07, 2022 (GLOBE NEWSWIRE) -- The "Computer System Validation ( CSV) 3 Day Virtual Seminar" training has been added to ResearchAndMarkets.com's offering.
This course is designed to completely immerse you in the principles, methods, and best practices of Computer System Validation (CSV).
You will learn about the regulations that impact your systems and gain hands-on practice writing validation documents. You will leave ready to lead efficient, effective, inspection-ready validation projects, whether you choose to follow a traditional waterfall or agile methodology.
Boot camp is tough and challenging. It is a three-day complete immersion in the validation process, including industry best practices and more recent advances in technology. Participants will complete hands-on validation activities through instruction, exercises, and case scenarios.
Registration Cost Includes:
- Checklist of documents and the direction for how to create
- Course binder
- Many exercises on Validation Plan, the Requirements Traceability Matrix, and the Validation Summary Report.
- Training Certificate
Please bring a laptop to boot camp. You will need internet access, spreadsheet and word processing applications and a PDF reader.
Learning Objectives
- Understanding of how to comply with key FDA and international CSV regulations and guidance, such as 21 CFR Part 11 and Annex 11
- The purpose of each validation deliverable and hands-on practice creating each deliverable, including the Validation Plan, Requirements Specification, Test Plan, Validation Tests (IQ, OQ, PQ), Trace Matrix, Test Summary, and Validation Report
- Comprehension of risk-based validation techniques and how to leverage these techniques to create efficient yet compliant validation approaches
- Appropriate validation strategies for many types of applications, including Cloud/SaaS, COTS, spreadsheets, and custom developed systems
- Awareness of best-practices and inspector expectations for computer system validation and software quality assurance (SQA) programs
Who Should Attend:
Personnel in the following roles will benefit:
- Information Technology Analysts
- Information Technology Developers and Testers
- Software Quality Assurance Professionals
- QC/QA Managers and Analysts
- Analytical Chemists
- Compliance and Audit Managers
- Laboratory Managers
- Automation Analysts
- Manufacturing Specialists and Managers
- Supply Chain Specialists and Managers
- Regulatory Affairs Specialists
- Regulatory Submissions Specialists
- Risk Management Professionals
- Clinical Data Analysts
- Clinical Data Managers
- Clinical Trial Sponsors
- Computer System Validation Specialists
- GMP Training Specialists
- Business Stakeholders/Subject Matter Experts
- Business System/Application Testers
- Vendors responsible for software development, testing and maintenance
- Vendors and consultants working in the life sciences industry who are involved in computer system implementation, validation and compliance
Key Topics Covered:
AGENDA - Day 1
Module 1: Computer System Validation (CSV) Regulations
- FDA Regulations and Guidance
- Other Regulations and Guidance (EMA, ICH, EU, MHRA, PIC/S)
- Exercise: Exploring the Regulations using the fda.gov website
Module 2: Computer System Validation Method and Models
- Validation, verification, and qualification
- Common SDLCs
- GAMP 5 "V" Model
- COTS, Cloud, SaaS, PaaS, IaaS
- Spreadsheet Validation
Break 15 mins
Module 3: 21 CFR Part 11
- 21 CFR Part 11 Guidance
- Electronic records/signatures requirements
- Exercise: FDA Guidance for ER/ES
Data Integrity and Governance
Session End Time : 05:00 PM EDT
AGENDA - Day 2
Module 4: Validation Planning
- Validation Strategy Document
- Validation Strategy Components
- Rationale for Validation Testing
- GAMP 5 System Categorization
Module 5: Risk-Based Validation
- Risk assessment
- Risk mitigation
- Exercise: Validation Plan writing
Break
Module 6: Requirements
- Requirements development
- User Requirements Specification (URS)
- Functional Requirements Specification (FRS)
- Exercise: Requirements Interviews and URS/FRS writing
Module 7: System Design and Development
- System Design Configuration (SDS)
- Configuration Management Specification (CMS)
Module 8: IQ, OQ, PQ Protocols, and Execution
- Validation testing process
- IQ purpose and contents
- OQ purpose and contents
- PQ purpose and contents
Module 9: Validation Testing Plan
- Principles of validation testing
- Testing techniques
- Testing Plan purpose and contents
- Exercise: Testing Plan writing
Module 10: IQ, OQ, PQ Protocols
- Protocol structure and contents
- Objective evidence
- Test writing best practices
- Test structure best practices
- Exercise: IQ/OQ/PQ writing
Module 11: Test Execution
- Test execution best practices
- Validation failure documentation
- Exercise: Validation test execution
Session End
AGENDA - Day 3
Module 12: Requirements Traceability Matrix (RTM)
- Trace Matrix purpose and contents
- Exercise: Trace Matrix writing
Module 13: Test and Validation Reports
- Test Summary purpose and contents
- Validation Report purpose and contents
- Exercise: Validation Summary Report writing
Module 14: Change Management
- Maintaining validation status
- Change control processes
- Security and Access
- Audit Trail Review
- Incidence Reporting
- Periodic System Review
Module 15: System Retirement
- Record retention
- Retirement challenges
Break 15 mins
Module 16: FDA Warnings Letters
- Current Trends in Compliance and Enforcement
- Case Study: FDA enforcement
- Exercise: Be the Consultant
Module 17: Q/A Session & CSV Exam
- Activity: Exam Preparation
- Final Exam
- Q/A Session with the Course Instructor
Session End
For more information about this training visit https://www.researchandmarkets.com/r/igihmb
