ComplianceOnline Announces Seminar on Computer System Validation

Top Quote ComplianceOnline, the leading GRC advisory network, and renowned regulatory affairs expert David Nettleton will conduct a two day seminar on FDA compliant computer system validation. End Quote
  • (1888PressRelease) January 05, 2013 - Palo Alto, CA, USA - ComplianceOnline, the leading governance, risk and compliance advisory network with over 500 experts in various regulatory subjects, today announced a seminar on Computer System Validation - Reduce Costs and Avoid 483s. The two day long seminar led by regulatory affairs expert David Nettleton will be held on February 7- 8, 2013 in the Phoenix, AZ.

    Lack of proper system validation is one of the major reasons for warning letters and 483s in most of the FDA regulated industries. This two day seminar will provide tools needed to develop and implement effective computer system validation processes to gain maximum productivity and reduce cost by as much as two thirds.

    For more information or to register for the seminar, please Click here .

    Seminar instructor 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 196 mission critical laboratory, clinical, and manufacturing software implementation projects.

    During the two day interactive seminar, Mr. Nettleton will discuss proven techniques for reducing costs and time associated with computer system implementation and maintenance in regulated environments. He will explain the latest computer system industry standards for data security, data transfer and audit trails with a 10-step risk-based approach to computer system validation. The seminar will give the attendees an understanding of how 21 CFR Part 11 and HIPAA electronic security regulations for patient medical records fit into the validation process. He will also discuss recent FDA trends and how to streamline SOP authoring, revision, review, and approval.

    The seminar will be beneficial for regulatory, clinical and IT professionals working in healthcare, clinical trial, biopharmaceutical and medical device sector that uses computer systems to perform their job functions. It will provide valuable guidance to Regulatory Affairs personnel, OA/QC personnel, IT/IS personnel, Software Managers, Project Managers, Software vendors and suppliers on effective computer system validation.

    Date: Thursday, February 7 and Friday, February 8, 2013, 8.30 AM- 4.30 PM MST

    Venue & Location: Courtyard Phoenix Camelback, AZ
    Registration Cost: $1,299.00 per registration
    Early bird discounts: For discounts on early registrations, please Click here .
    Register by phone: Please call our customer service specialists at +1-650-620-3937 or email to customercare ( @ ) complianceonline dot com

    For more information on ComplianceOnline or to browse through our trainings, please visit our website

    About ComplianceOnline
    ComplianceOnline is a leading provider of regulatory/compliance trainings for companies and professionals in regulated industries. ComplianceOnline has successfully trained over 20,00 professionals from 3,000 companies to comply with the requirements of regulatory agencies. ComplianceOnline is headquartered in Palo Alto, California and can be reached at

    For more information please contact:
    A Reuben Bernard
    Manager of Program Marketing
    2600 E Bayshore Rd
    Palo Alto CA USA 94303
    650-620-3937 phone
    650-963-2530 fax
    reuben ( @ ) complianceonline dot com

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