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Webinar on Best Practices in Preparation for an FDA Computer System Audit

  March 04, 2016  

Compliance Trainings, Online

Description :

The Webinar will discuss the importance of preparing for and participating in a computer system validation audit by regulatory agencies. Regulatory agencies fully expect companies to comply with the computer system validation guidelines that were established in 1983 and have evolved over the last thirty years to align with changes in technology and best practices developed by industry, including the inclusion of risk assessment as a critical component of validation.

Validation of computer systems in the regulatory environment must be a continuous rather than a discrete process. When auditing, regulatory agencies will expect you to have adequately planned and executed your computer system validation effort, and continue to maintain your system in a validated state.

There are specific best practices to be followed that will ensure you are fully prepared to defend your program and prove that you have thoroughly validated your computer systems that are subject to regulatory scrutiny. Being prepared will ensure a much easier interaction with the regulatory agency and will minimize the time and cost of the audit. A company’s readiness may also minimize the risk of findings and citations by showing the auditors that you have done due diligence and are able to respond adequately to all questions and requests for information in a timely manner.

Areas Covered in the Session :

Describe the key components and importance of regulatory audits of validated computer systems

Discuss best practices for preparing for a computer system validation audit by a regulatory agency

Provide examples of the documentation you can prepare to minimize risk and ensure your audit is successful

Discuss best practices for participating in a computer system validation audit by a regulatory agency

Provide examples of what you can do during the audit to minimize risk, time and overall cost

Discuss best practices for developing a positive relationship with regulatory agency auditors and building a reputation for preparedness, thoroughness and integrity

Interactive Q&A Session

Who Will Benefit:

This webinar is intended for those working in FDA-regulated industries, including pharmaceutical, medical device, biological, animal health and tobacco. Functions that are applicable include research and development, manufacturing, Quality Control, distribution, clinical testing and management, adverse events management and post-marketing surveillance.

You should attend this webinar if you are responsible for planning, executing or managing the implementation of any system governed by FDA regulations, or if you are maintaining or supporting such a system. Examples of who will benefit from this webinar include:

Compliance and Audit Managers

Information Technology Analysts

Information Technology Developers and Testers

QC/QA Managers and Analysts

Clinical Data Managers and Scientists

Analytical Chemists

Laboratory Managers

Automation Analysts

Computer System Validation Specialists

GMP Training Specialists

Business Stakeholders/Subject Matter Experts

Business System/Application Testers


This webinar will also benefit any consultants working in the tobacco or life science industries who are involved in computer system implementation, validation and compliance.

Organized by: Compliance Trainings
Invited Speakers: Carolyn Troiano has more than 30 years of experience in computer system validation in the pharmaceutical, medical device, animal health, tobacco and other FDA-regulated industries. She is currently an independent consultant, advising companies on computer system validation and large-scale IT system implementation projects.
Deadline for Abstracts: 2016-03-14

For more information about this event please visit



To register this webinar


E-mail: suzzane.d@compliancetrainings.com
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