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Organizational Change Management (OCM) for FDA-Regulated Computer Systems

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Course Description:

         The key challenge for many users and others working to validation computer systems involves their ability, or lack thereof, to control data and information. If processes change such that users who had a part in the review and approval of data and/or information are no longer required to participate, they may feel insecure, both about how well data integrity, identity and accuracy is maintained, and about their own job stability. It is not uncommon for newer systems to take over the role of automatic matching or checking that was once done by a human. Once thoroughly tested, the process eliminates the potential for human error, while reducing the time and cost associated with it.

         A key challenge to IT and other implementation and support personnel in Organizational Change Management is the degree to which they must participate in any validation effort. IT resources that are not typically involved in FDA-regulated systems may not have the training required to provide implementation or maintenance support. It is critical that if they are involved, they buy into the concept that they must do this work in a compliant manner, and that there is no room for short-cuts.

         Management may also erect barriers to change. If they no longer have visibility into data/information, or if their data/information is now visible to others who previously could not see it, they will have some concerns. They must have a thorough understanding of the level of security applied and knowledge of exactly who has what type of access to it. In addition, while they may have received reports in the past, they may now be required to get this information directly from the system by logging in and running a query or report electronically. They will have to be assured that the data sources are the same, the integrity is maintained through reporting, and the reports are in real-time, meaning they are always up-to-date. If this is not the case, that also must be conveyed to them.

         The Organizational Change Management goal is to communicate effectively the impact of change to users and others, and to allay any concerns they may have about the future. Identifying these is critical to avoid complaints and non-compliance later on. In extreme OCM cases, there could be sabotage, which could sideline any effort quickly and destroy the credibility of the team.

Why should you Attend?

         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 changes that will impact the organization will be identified clearly and will be minimized to eliminate additional cost and wasted time.

         There is an enormous body of documentation and information available that can be overwhelming. This Organizational Change Management course will provide a condensed overview of the practices that deliver the best results by directing the attendees to the most critical and cost-effective of methods, techniques and tools available.

         You should attend this Organizational Change Management 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.

Areas Covered:

This 90 mins OCM course will include:
  • 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
  • Discuss the importance of communicating early and often to assure the organization their opinions and concerns are being addressed satisfactorily
  • Learn how to differentiate between "real" and "perceived" issues to eliminate the "boogey-man" and focus on real, tangible changes
  • Learn how to leverage these practices to employ them during any process change experienced by the organization
  • Understand the additional training that must be provided to business and IT staff involved in the change process
  • Discuss the communications necessary to ensure that users are employing the appropriate changes to processes vs. using "shadow systems," in which case they may end up duplicating work and continuing to introduce human error into the mix
  • Q&A

Who will Benefit?

Individuals with the following roles in an FDA-regulated organization will benefit from this Organizational Change Management webinar:

  • Information Technology Analysts
  • Information Technology Developers and Testers
  • QC/QA Managers and Analysts
  • Analytical Chemists
  • Compliance and Audit Managers
  • 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 life sciences industry who are involved in computer system implementation, validation and compliance.


Target Industries/Associations/Societies
  • Pharmaceutical
  • Biotechnology
  • Medical Device
  • Tobacco
  • e-Liquid/Vapor
  • Cigar

Any company regulated by FDA, or doing work that is governed by FDA requirements. This includes consulting firms, vendors and others.

Registration Options



Max 5 participants from a single location with 1 Dial-in.


Max 10 participants from a single location with 2 Dial-in.


Avail 12 months unlimited access for a single user.


Material shipped within 15 days post webinar completion & get life time access for unlimited participants.



Avail recording + Attend live session for a single participant.


Unlimited participants for max 5 locations.


Tags


Organizational Change Management, OCM, FDA Regulated Computer Systems, FDA Requirements, Computer System Validation, FDA Regulated Industries, Clinical Testing and Management,

Speaker Details

Carolyn  Troiano

Carolyn Troiano

FDA/Medical Device Consultant

Carolyn Troiano  has more than 35 years of experience in computer system validation and compliance in the pharmaceutical, medical device, tobacco and other FDA-regulated industries.  

Refund Policy



Participants/Registrants for our live events, may cancel up to 72 hours prior to the start of the live session and ComplyArena will issue a letter of credit to be used towards any of ComplyArena's future events. The letter of credit will be valid for 12 months.

ComplyArena will process refund in cases where the event has been cancelled and is not rescheduled within 90 days from the original scheduled date of the webinar. In case if a live webinar is cancelled, participants/registrants may choose between recorded version of the course or a refund. Refunds will not be processed to participants who do not show up for the webinar. A webinar may be cancelled due to unavoidable circumstances, participants will be notified 24 hours before the scheduled start of the event. Contact us via email: admin@complyarena.com or call +1-888-222-5917 (Toll Free).