Data - Governance, Risk, Compliance

10:30 AM ET | 07:30 AM PT | 09:30 PM CT Duration 90 Minutes

Webinar Includes : All the training handouts , certificate ,Q/A and 90 mins Live Webinar

"Eleonora Babayants is a documentation management professional and hands-on consultant with over 25 years of experience in documentation and records management"

Documentation is a critical tool for ensuring GxP/GMP compliance

Description

GxP/GMP regulations are required to be used in regulated industries such as food and beverages, pharmaceutical, medical devices, and cosmetics.

Documentation is a critical tool for ensuring GxP/GMP compliance. In order to maintain documentation in GxP/GMP compliant manner, information governance should be developed and implemented.

Data security is the high priority in any organization but especially in a regulated industry.

E-Discovery preparedness makes it imperative for organizations to develop an enterprise wide strategy to manage the volume of electronic information. The discovery process affects many individuals in an organization, not just lawyers and others involved in discovery, but also IT professionals and records managers who have to be prepared to produce electronic content for discovery and litigation.

Crisis preparedness is the high priority in any organization but especially in a regulated industry.

Why Should You Attend

In the regulated environment which must be GxP/GMP compliant, document control is the cornerstone of the quality system. It is so important that if an external audit identifies deficiencies in the document control system, the entire organization can be shut down.

Documentation is the key to GMP compliance and ensures traceability of all development, manufacturing, and testing activities. Documentation provides the route for auditors to assess the overall quality of operations within a company and the final product.

In order to maintain documentation in GxP/GMP compliant manner, information governance procedures should be developed and implemented. In the regulated industries, manufactures are required to use a change control procedure.

It is imperative to secure data, prepare for e-discovery, and be ready if crisis strikes.

When all procedures and systems are set up, change management and user adoption become necessary.

Do you know how to properly manage and govern your documentation so that your organization is GxP/GMP compliant?

Learn how to manage and govern documents as well as IT systems in compliance with GxP/GMP requirements and be able to pass quality audit.

Is your organization ready for e-discovery and do you have crisis preparedness in place? Do you have change management and user adoption strategy?

Learn how to secure your data, prepare for e-discovery and crisis, and how to develop and implement change management strategy.

Learning Objectives

 

GxP/GMP regulations are required to be used in regulated industries such as food and beverages, pharmaceutical, medical devices, and cosmetics.

Documentation is a critical tool for ensuring GxP/GMP compliance. In order to maintain documentation in GxP/GMP compliant manner, information governance should be developed and implemented.

Data security is the high priority in any organization but especially in a regulated industry.

E-Discovery preparedness makes it imperative for organizations to develop an enterprise wide strategy to manage the volume of electronic information. The discovery process affects many individuals in an organization, not just lawyers and others involved in discovery, but also IT professionals and records managers who have to be prepared to produce electronic content for discovery and litigation.

Crisis preparedness is the high priority in any organization but especially in a regulated industry.

In this webinar, you will learn the framework of GxP/GMP regulations, change management procedures, information governance procedures, and how to implement them.

You will also learn how to implement data security, e-discovery and crisis preparedness.

Areas Covered

  • What is Information Governance?
  • Information Governance Procedures
  • Information Governance Implementation
  • Information Governance in Document Management Systems
  • Social Media Management and Information Governance
  • GxP/GMP and Change Control Procedure

Who will Benefit

  • Pharmaceutical 
  • Medical Devices
  • Food
  • Cosmetics
  • Any other regulated industry

Industries who can attend

This 90-minute online course is intended for professionals in the Pharmaceutical, Clinical Data Management SaaS companies, and medical device companies . Although not presently stated in the draft , the same guide could be used by FDA Regulated Industries personnel


Speaker Profile

Eleonora Babayants

Galaxy Consulting Founder and President Eleonora Babayants is a documentation management professional and hands-on consultant with over 25 years of experience in documentation and records management, document control, regulatory compliance, internal and external auditing, electronic document management systems, information governance, and change management.

Eleonora’s past work includes development and implementation regulatory compliance processes and procedures, leading implementation and administration of document control systems in full compliance with regulatory requirements, enabling enterprise search, improving systems information architecture, creating and implementing users training programs.

She led electronic document management systems selection and deployment, administered and supported these systems, web information portals, knowledge base applications, recommended and implemented re-structuring of the content and the information architecture of these systems. She worked very closely with IT to do feasibility assessment and to capture users’ requirements. She wrote technical documents and created documents templates.

Eleonora’s experience spans multiple industries including biomedical, pharmaceutical, and medical devices companies.

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