PRN: Two Day Seminar: Computer System Validation Seminar - Reduce Costs and Avoid 483s (Philadelphia, PA, United States - May 8-9, 2017) - Research and Markets

03/mar/2017 14:01:15 PR Newswire Turismo Contatta l'autore

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Two Day Seminar: Computer System Validation Seminar - Reduce Costs and Avoid 483s (Philadelphia, PA, United States - May 8-9, 2017) - Research and Markets


DUBLIN, Mar 3, 2017 /PRNewswire/ --

Research and Markets has announced the addition of the "Computer System Validation - Reduce Costs and Avoid 483s" conference to their offering.

This Computer System Validation Training 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 Computer System Validation Training 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.


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

  • Introduction to the FDA (1 hr)
  • 21 CFR Part 11 - Compliance for Electronic Records and Signatures (4 hr)
  • HIPAA Compliance for Electronic Records (30 Min)
  • The Five Keys to COTS Computer System Validation (30 Min)
  • The Validation Team (30 Min)

Day 02 (8:30 AM - 3:30 PM)

  • Ten-Step Process for COTS Risk-Based Computer System Validation (1 hr)
  • How to Write Requirements and Specifications (30 Min)
  • How to Conduct a Hazard Analysis/Risk Assessment-Exercise (30 Min)
  • Software Testing (1 hr)
  • System Change Control (30 Min)
  • Purchasing COTS Software (30 Min)
  • Cost Reduction Without Increasing Regulatory or Business Risk (1 hr)

For more information about this conference visit

Media Contact:

Research and Markets

Laura Wood, Senior Manager

For E.S.T Office Hours Call +1-917-300-0470

For U.S./CAN Toll Free Call +1-800-526-8630

For GMT Office Hours Call +353-1-416-8900

U.S. Fax: 646-607-1907

Fax (outside U.S.): +353-1-481-1716


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