This webinar is intended for those working in the 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.
Areas Covered in the Session :
Linking data governance activities and investments to corporate drivers, strategies and compliance
Establish data governance program objectives, decision-making organizational structures and assigned roles and responsibilities that fit within the organizational culture
Understand the role of data owners vs. data stewards
Understand the criticality of data identity, trust, security, integrity, accessibility, reliability and consistency
Designing data governance processes that encompass people, processes and technology
Understand the policies and procedures necessary to support the data governance framework
Who Will Benefit:
Examples of who will benefit from this webinar include:
Information Technology Analysts
Information Technology Developers and Testers
QC/QA Managers and Analysts
Compliance and Audit Managers
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 life sciences industry who are involved in computer system implementation, validation and compliance.
15 Jul 2016 @ 01:00 pm
15 Jul 2016 @ 02:00 pm
Duration: 1 hours
Timezone: GMT -5:00