This Event has Passed
Wednesday, September 17, 2014
10:00 AM - 11:00 AM
10:00 AM - 11:00 AM See all dates and Times
http://complianzworld.com/Webinars.aspx?TopicId=489&Sub=How-to-approach-organizational-change-management-when-automating-processes-
Description: We will discuss the importance of applying industry best practices for organizational change management as they relate to the planning, execution and validation of systems to comply with FDA requirements. Most system implementation and upgrade efforts involve change, as companies strive to improve their business processes to achieve greater efficiency and effectiveness.
Course Objective:
You should attend this seminar 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 as changes are made.
Course Outline:
• Gain an understanding of the various factors that impact organizations when implementing new or updated computers
• Discuss the best practices necessary to identify challenges and concerns to minimize impact
• Learn how to communicate effectively to reduce the potential for sabotage, erection of barriers to change, and other means of canceling out the positive effect of the intended change
• Understand that each user or manager may perceive different challenges to their daily work and may begin to feel insecure about their position in the organization
Target Audience:
• Information technology analysts,
• QC/QA managers and analysts,
• Clinical data managers and scientists,
• Analytical chemists,
• Compliance managers,
• Lab managers,
• Automation analysts,
Speaker profile : Carolyn Troiano
Carolyn Troiano has more than 25 years of experience in computer system validation in the pharmaceutical, medical device, animal health and other FDA-regulated industries. She is currently the ERP (Enterprise Resource Planning).
Event Price Tags :
$ 229.00 Single Attendee
$ 749.00 Group – Max 10 Attendees per location
$ 269.00 Access Recorded Version online
$ 399.00 Buy Training CD-DVD
For More Details or Enrollment Or Registration :
Contact : complianzworld
Phone : +1-866-978-0800
Fax : +1-888-883-7697
Course Objective:
You should attend this seminar 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 as changes are made.
Course Outline:
• Gain an understanding of the various factors that impact organizations when implementing new or updated computers
• Discuss the best practices necessary to identify challenges and concerns to minimize impact
• Learn how to communicate effectively to reduce the potential for sabotage, erection of barriers to change, and other means of canceling out the positive effect of the intended change
• Understand that each user or manager may perceive different challenges to their daily work and may begin to feel insecure about their position in the organization
Target Audience:
• Information technology analysts,
• QC/QA managers and analysts,
• Clinical data managers and scientists,
• Analytical chemists,
• Compliance managers,
• Lab managers,
• Automation analysts,
Speaker profile : Carolyn Troiano
Carolyn Troiano has more than 25 years of experience in computer system validation in the pharmaceutical, medical device, animal health and other FDA-regulated industries. She is currently the ERP (Enterprise Resource Planning).
Event Price Tags :
$ 229.00 Single Attendee
$ 749.00 Group – Max 10 Attendees per location
$ 269.00 Access Recorded Version online
$ 399.00 Buy Training CD-DVD
For More Details or Enrollment Or Registration :
Contact : complianzworld
Phone : +1-866-978-0800
Fax : +1-888-883-7697
