ComplianceOnline Announces Seminar on Computer System Validation to be held in CA and PA

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ComplianceOnline, the leading GRC advisory network and, subject matter expert, David Nettleton, will conduct a two day seminar on FDA compliant computer system validation.

Computer System Validation - Reduce Costs and Avoid 483s

Computer System Validation - Reduce Costs and Avoid 483s

Computer System Validation - Reduce Costs and Avoid 483s: 2-Day In-Person Seminar

Led by well-known FDA compliance specialist David Nettleton, ComplianceOnline’s on-demand seminar on computer system validation (CSV) returns to California and Philadelphia in 2017. The two-day training program will address latest computer system industry standards for data security, data transfer, audit trails, electronic records and signatures, software validation, and computer system validation.

Given the constant updates in the industry, each session in the seminar will cover these industry updates and focus on best practices to avoid 483s and Warning Letters. From learning how to buy COTS software and qualifying vendors to change control methods that allow quick and safe system evolution, this in-person training will assist regulatory affairs personnel, software managers, QA/ QC teams and others within an organization.

The 2016 ComplianceOnline CSV seminar participation from various healthcare and pharma organizations, such as Cancer Treatment Centers of America, Mylan LLC, Vital Therapies, Inc., BioLife Solutions, Asterias BioTherapeutics and others, have made the event an industry platform to reckon with.

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 230 mission critical laboratory, clinical, and manufacturing software implementation projects.

During the seminar, Mr. Nettleton will also review recent FDA inspection trends and discuss how to streamline document authoring, revision, review, and approval, allowing participants to implement his recommendations and successfully completing FDA inspections.

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

Dates: Thursday, February 2, 2017 (8.00 AM- 5.00 PM) and Friday, February 3, 2017 (8.30 AM- 3.30 PM)
Thursday, April 27, 2017 (8.00 AM- 5.00 PM) and Friday, April 28, 2017 (8.30 AM- 3.30 PM)
Thursday, June 15, 2017 (8.00 AM- 5.00 PM) and Friday, June 16, 2017 (8.30 AM- 3.30 PM)
Location 1: San Diego, CA
Location 2: Philadelphia, PA
Location 3: San Diego, CA
Registration Cost: $1,999.00 per registration
Early bird discounts: For discounts on early registrations, please click here.
Register by phone: Please call our customer service specialists at +1-888-717-2436 or email to customercare(at)

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 35,000 professionals from 9,000 companies to comply with the requirements of regulatory agencies. ComplianceOnline is headquartered in Palo Alto, California and can be reached at ComplianceOnline is a MetricStream portal. MetricStream ( is a market leader in Enterprise-wide Governance, Risk, Compliance (GRC) and Quality Management Solutions for global corporations.

For more information please contact:

A Reuben Bernard
Associate Director - ComplianceOnline
2600 E Bayshore Rd
Palo Alto CA USA 94303
Phone - +1-650-238-9656 | +1-888-717-2436
Fax - 650-963-2556
Mail: reuben(at)

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A Reuben Bernard
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