Reduce costs for compliance with data integrity (com) A

Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR

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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.
It details the requirements for HIPAA Protect Health Information (PHI)
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).

Seminar Fee Includes:
Lunch
AM-PM Tea/Coffee
Seminar Material
USB with seminar presentation
Hard copy of presentation
Attendance Certificate
$100 Gift Cert for next seminar

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 HIPAA expands Part 11 compliance
• 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 will Benefit:

GMP, GCP, GLP, regulatory professionals
QA/QC
IT
Auditors
Managers and directors
Software vendors, SaaS hosting providers

AGENDA

Day 01(8:00 AM - 5:00 PM)

08.00 AM - 08.30 AM: Registration
08.30 AM: Session Start
Introduction to the FDA (1 hr)
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 (4 hr)
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.
HIPAA Compliance for Electronic Records (30 Min)
How Part 11 and HIPAA interrelate
What are the additional requirements for patient data
The Five Keys to COTS Computer System Validation (30 Min)
The Who, What, Where, When, and Why of CSV
The Validation Team (30 Min)
How to select team members
How to facilitate a validation project

Day 02(9:00 AM - 3:30 PM)

Ten-Step Process for COTS Risk-Based Computer System Validation (1 hr)
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).
How to Write Requirements and Specifications (30 Min)
Workshop for writing requirements and then expanding them for specifications
How to Conduct a Hazard Analysis/Risk Assessment-Exercise (30 Min)
Step-by-step instructions for performing and documenting a risk assessment, and how to use the results to reduce validation documentation.
Software Testing (1 hr)
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 (30 Min)
How to meet the requirements of the EU GDPR
Purchasing COTS Software (30 Min)
How to purchase COTS software and evaluate software vendors
Cost Reduction Without Increasing Regulatory or Business Risk (1 hr)
How to save money
How to increase quality
How to increase compliance with less documentation

SPEAKER

David Nettleton
FDA Compliance Specialist, Computer System Validation

Computer System Validation’s principal, David Nettleton is an industry leader, author, and teacher for 21 CFR Part 11, Annex 11, HIPAA, 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 230 mission critical laboratory, clinical, and manufacturing software implementation projects. His most popular book is Risk Based Software Validation - Ten easy Steps, which provides fill-in-the-blank templates for completing a COTS software validation project.

Please contact the community manager Marilyn (marilyn.b.turner@nyeventslist.com ) below for:

- Multiple participant discounts
- Price quotations or visa invitation letters
- Payment by alternate channels (PayPal, check, Western Union, wire transfers etc)
- Event sponsorships
NO REFUNDS ALLOWED ON REGISTRATIONS
Service fees included in this listing.
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