DUBLIN: The "21 CFR Part 11 Compliance for SaaS/Cloud Application (ONLINE EVENT: August 6-7, 2025)" has been added to ResearchAndMarkets.com's offering.

Join the “21 CFR Part 11 Compliance for SaaS/Cloud Application” live online event on August 6–7, 2025. This two-day training helps healthcare, biotech, and IT professionals reduce validation costs, avoid FDA 483s, and ensure compliance with electronic record and signature regulations. Includes real-life examples, templates, and GDPR guidance.

• 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.

Learning Objective

• 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
• IT
• Auditors
• Managers and directors
• Software vendors, SaaS hosting providers

Course Agenda:

Day 1

• Introduction to the FDA
  • How the regulations help your company to be successful
  • Which data and systems are subject to Part 11
• 21 CFR Part 11/Annex 11 - Compliance for Electronic Records and Signatures
  • 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.
• The Five Keys to COTS Computer System Validation
  • The Who, What, Where, When, and Why of CSV
• The Validation Team
  • How to select team members
  • How to facilitate a validation project
• Ten-Step Process for COTS Risk-Based Computer System Validation

DAY 02

• Software demonstrations and discussions
• Ten-Step Process for COTS Risk-Based Computer System Validation
  • 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)
• How to Write Requirements and Specifications
  • Workshop for writing requirements and then expanding them for specifications
• How to Conduct a Hazard Analysis/Risk Assessment-Exercise
  • Step-by-step instructions for performing and documenting a risk assessment, and how to use the results to reduce validation documentation.
• Software Testing
  • Reduce testing by writing test cases that trace to elements of risk management.
  • How to write efficient test cases
• How to write a Data Privacy Statement
  • How to meet the requirements of the EU GDPR
• Purchasing COTS Software
  • How to purchase COTS software and evaluate software vendors
• Cost Reduction Without Increasing Regulatory or Business Risk
  • How to save money
  • How to increase quality
  • How to increase compliance with less documentation

For more information about this training visit https://www.researchandmarkets.com/r/oroppz

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Fonte: Business Wire