GDPR 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"

Create better data protection policies and to hold the organizations

Description

The General Data Protection Regulation (GDPR), introduced by the European Union, took effect on May 25, 2018. This regulation has changed how organizations handle personal data of data subjects, including customers, employees, and prospects. Organizations had to revamp their processes and systems to be compliant with the new stringent data protection standards.

The purpose of the GDPR is to create better data protection policies and to hold the organizations that handle personal data more accountable.

But the transition isn’t easy. The new processes have to be systemic and self-serving rather than ad hoc, manual, and intrusive. This webinar would help organization which are affected by the GDPR. It includes the comprehensive and structured plan to achieve GDPR compliance

Why should you attend

With the introduction of the GDPR, organizations are under intense scrutiny regarding how they use the personal data of customers, employees, and prospects. Non-compliance can lead to heavy fines, so it is imperative for organizations to understand the data that they collect and use it only in the manner approved by the data subject.

GDPR lays out a set of rules with which organizations need to be compliant. Together, these articles warrant that organizations handle personal data with sensitivity, protect it, control data quality, and ensure that the data subjects are aware of how it’s used.

It is very important for organization to implement systematic processes to be compliant with GDPR to avoid fines.

In this webinar, you will learn steps to achieve GDPR compliance.

Learning Objectives

GDPR applies to data subjects in the EU, even when data is processed by organizations operating in outside jurisdictions like the United States, Asia Pacific, Middle East, and Africa. Non-compliance with the GDPR may result in huge fines.

In this webinar, we will present the structured plan to achieve GDPR compliance. You will learn:

  • How do develop processes, standards, and controls
  • How to manage data and improve its quality
  • How to establish data collection
  • How to define acceptable data use
  • How to conduct vendor risk
  • How to manage end-user computing
  • How to govern lifecycle of information
  • And other measures you need to take to achieve GDPR compliance.

Areas Covered

  • Processes, standards, and controls for GDPR compliance
  • Data management and its quality improvement
  • Data collection
  • Acceptable data use
  • Vendor risk
  • End-user computing
  • Governing lifecycle of information
  • And other areas you need to take care of to achieve GDPR compliance

Who will Benefit

  • Quality Assurance
  • Documentation Managers
  • Records Managers
  • Document Control
  • Compliance
  • Medical Affairs
  • IT

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.

Back to Top