Seminar Information

21 CFR Part 11 compliance for software validation and SaaS/Cloud - Brazil

21 CFR Part 11 compliance for software validation and SaaS/Cloud - Brazil, Sao Paulo, Brazil
Seminar Title
21 CFR Part 11 compliance for software validation and SaaS/Cloud - Brazil
Event Type
Seminar Date
22-06-2017 to 23-06-2017
Sao Paulo, Brazil

Publish / Maintain / Marketing / Hosted By
Organization Name / Organize By
NetZealous DBA as GlobalCompliancePanel
Organizing/Related Departments
NetZealous DBA as GlobalCompliancePanel
Organization Type
Event Organizing Company
Seminar Category
Non Technical
Seminar Level
Related Industries



Sao Paulo, Brazil


  • This interactive two-day course explores proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments.
  • Many companies are outsourcing IT resources and getting involved with 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. It is the regulated company that wants to avoid FDA form 483s and warning letters. The seminar is intended for regulated companies, software vendors, and SaaS/Cloud providers.
  • 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.
  • 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.
  • This seminar will help you 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.
  • Finally, the instructor reviews recent FDA inspection trends and discusses how to streamline document authoring, revision, review, and approval.
  • This course benefits anyone that uses 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.

Course Objectives:

  • Understand what is expected in Part 11 and Annex 11 inspections
  • Avoid 483 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:

  • QA, IT, management
  • all GxP system users

Others Details

For more details and updates please visit seminar website

Registration Fees
Registration Fees Details
Price: $1,095.00 (Seminar Fee for One Delegate) Register for 5 attendees Price: $3,285.00 $5,475.00 You Save: $2,190.00 (40%)* Until May 10, Early Bird Price: $1,095.00 From May 11 to June 20, Regular Price: $1,295.00 For more details and updates please visit seminar website
Registration Ways
Sao Paulo, Brazil [visit seminar website]  Pin/Zip Code : 01016-020
Official Email ID
NetZealous DBA as GlobalCompliancePanel

161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA.

[email protected]

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