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Live Webinar FDA Compliance and Mobile Applications

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Deadline: May 02, 2018 | Date: May 02, 2018

Venue/Country: Online, U.S.A

Updated: 2018-04-16 21:33:43 (GMT+9)

Call For Papers - CFP

Live Webinar FDA Compliance and Mobile Applications

Date: 01:00 PM EDT | 10:00 AM PDT | 12:00 PM CDT Duration 90 Minutes


Computer system validation has been regulated by FDA for more than 30 years, as it relates to systems used in the manufacture, testing, distribution and management of a product in the pharmaceutical, biotechnology, medical device, tobacco and other regulated industries.

As a major part of the computer system validation effort, an FDA-regulated company must ensure that all validation documentation is prepared in accordance with the Agency’s guidelines. Having the right documents and preparing and managing them according to best industry practices is critical to validation success.

Effective and compliant computer system validation is critical to any pharmaceutical or FDA-regulated organization. During the past 30 years, best practices that have been developed will ensure that the cost of building and managing a computer system validation program will be minimized.

Why should you attend

You should attend this seminar if you are responsible for planning, executing or managing the validation of a system governed by FDA regulations that incorporates mobile software or devices into the system structure.

Upon completion of this session, attendees will have an understanding of computer system validation planning, execution and management concepts, in terms of how these efforts are to be adequately documented to meet FDA requirements. They will understand the steps required for documenting the validation process, along with the key documentation associated with maintaining the systems in a validated state, while minimizing costs. The attendees will have a good grasp of how to leverage these practices across all systems by creating a standardized program.

Areas Covered

• Gain an understanding of how mobile applications should be handled when performing validation work

• Understand the best practices for maintaining a mobile application in a validated state

• Discuss the best practices necessary to ensure all systems, including mobile applications, are validated appropriately

• Learn how to develop the appropriate computer validation strategy when dealing with mobile applications to ensure a good balance of cost vs. risk

• Understand how to effectively document the process of computer system validation, and maintain current information about the various systems in your organization, as they begin to include mobile applications

• Learn how to gain information about trends in validation of mobile applications, as industry progresses and new best practices emerge

• Understand some of the key “pitfalls” to avoid when applying the concepts of computer system validation to mobile applications

• Q&A

Who will Benefit

Professionals in the following industries may also benefit from the content:

• Pharmaceutical

• Medical Diagnostics

• Biotechnology

• Tobacco and Related (Vapor, e-Cigarette, Cigar, etc.)

• Animal Health

Any other FDA-regulated industry, plus any Life Science Consulting or Contracting firm

• Information technology managers and analysts

• QC/QA managers and analysts

• Clinical data managers and scientists

• Compliance managers

• Lab managers and staff

• Automation analysts

• Computer system validation specialists

• GMP training specialists

• Business stakeholders and individuals who are responsible for computer system validation planning, execution, reporting, compliance, and audit

• Consultants working in the life sciences, tobacco and related industries who are involved in computer system implementation, validation and compliance

Speaker Profile

Carolyn Troiano has more than 35 years of experience in computer system validation in the pharmaceutical, medical device, animal health and other FDA-regulated industries. She is currently managing a large, complex data migration, analytics and reporting program at a major financial institution.

During her career, Carolyn worked directly, or as a consultant, for many top-tier pharmaceutical companies in the US and Europe. She was responsible for computer system validation across all GxP functions at a major pharmaceutical company. Carolyn developed validation programs and strategies back in the mid-1980s, when FDA guidelines were first issued. She was an industry reviewer for 21 CFR Part 11, the FDA’s electronic record/electronic signature (ER/ES) regulation.

Price: $179 One Dial-in One Attendee | Corporate Live Recorded $279 One Dial In - Max 10 attendees |Group $399 Multiple locations upto 5 dial in | Recorded $249

Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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