21 CFR Part 11 Compliance for SaaS/Cloud Applications | September 17, 2015 8:30 AM - September 18, 2015 4:30 PM | Automation.com

21 CFR Part 11 Compliance for SaaS/Cloud Applications

Event Summary

DATE:
September 17, 2015 - September 18, 2015
LOCATION:
Philadelphia, PA 19107
COUNTRY:
USA
START DATE/TIME:
September 17, 2015 8:30 AM
END DATE/TIME:
September 18, 2015 4:30 PM
EVENT TYPE:
Training
HOST:
ComplianceOnline
PHONE:
6506203915
EMAIL:
[email protected]
WEBSITE:
Click here to Visit

Description

Course Description:
This interactive two-day course will explore proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments. Today, the FDA performs both GxP and Part 11 inspections, the Europeans have released an updated Annex 11 regulation that expands Part 11 requirements and companies must update their systems and processes to maintain compliance.

Many companies outsource IT resources and are involved in Software as a Service (SaaS) and cloud computing. These vendors are not regulated, and therefore, regulated companies must ensure compliance for both infrastructure qualification and computer system validation to avoid FDA form 483s and Warning Letters.

This course is intended for these regulated companies, software vendors, and SaaS/cloud providers. The seminar instructor will:

Address the latest computer system industry standards for data security,data transfer, audit trails, electronic records and signatures, software validation, and computer system validation.
Help participants understand the specific requirements associated with local and SaaS/cloud hosting solutions.
Illustrate the importance of validating the quality process and every computerized system used in laboratory, clinical, and manufacturing settings.
Demonstrate how to decrease software implementation times and lower costs using a 10-step risk-based approach to computer system validation.
Review recent FDA inspection trends and discuss how to streamline document authoring, revision, review, and approval.

Learning Objective:
Understand what is expected in Part 11 and Annex 11 inspections
Avoid 483s and Warning Letters
Learn how to buy COTS software and qualify vendors
Implement a computer system using risk-based validation to gain maximum productivity and reduce cost by as much as two thirds
Requirements for local, SaaS, and cloud hosting
How to select resources and manage validation projects
"Right size" change control methods that allows quick and safe system evolution
Minimize the validation documentation to reduce costs without increasing regulatory or business risk
Write test cases that trace to elements of risk management
Protect intellectual property and keep electronic records safe

Who will Benefit:
This course will benefit all who use computer systems to perform their job functions and is ideal for regulatory, clinical, and IT 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.

Regulatory Affairs
QA/ QC
IT/IS
Software Managers
Project Managers
Software vendors and suppliers


For Registration - http://www.complianceonline.com/computer-system-validation-reduce-costs-and-avoid-483s-seminar-training-80202SEM-prdsm?channel=automation


Note: Use coupon code 232082 and get 10% off on registration.

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