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Event :Quality Management and Quality Audit According to GxP/GMP Requirements

Date :Friday April 26th, 2019

Location :Hilton Irvine/Orange County Airport
18800 MacArthur Blvd
Irvine, United States

Type :Conference & Seminar - International audience

Accreditation :--


 

Further information

Editorial

In this webinar, the framework of GxP/GMP regulations, quality management system, and quality audit will be described. Attendees will Learn about different types of quality audits and how to properly prepare for them, what actions you need to take to ensure that your organization will pass an audit.

Objectives

GxP/GMP is about Quality Management System (QMS) where an organization needs to demonstrate its ability to consistently provide product that meets customer and applicable statutory and regulatory requirements.

There are few types of quality audits. One of them is GMP audit. GMP audit is very important and critical for an organization in a regulated industry. The preparations for the audit should be done properly before the audit. The primary objective of the audit is to demonstrate the compliance with GxP/GMP regulations. FDA can drop in anytime to perform an unannounced GMP audit or investigation. A GMP audit is conducted to check whether your organization complies with GxP/GMP and to identify if you have full control over your processes, facility, and quality management system (QMS).

Learn about GxP/GMP regulations and how they affect quality management system and quality audit. Learn about different types of quality audits and how to properly prepare for them, what actions you need to take to ensure that your organization will pass an audit.

Program

Areas Covered in the Webinar:

  • GxP/GMP Framework
  • Quality Management System
  • Quality Audit

Speakers

Eleonora Babayants

Eleonora Babayants
Founder and President, Galaxy Consulting

Eleonora Babayants - Founder and President Galaxy Consulting, 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, knowledgebase 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, medical devices, food and beverages companies.

 
 

Location

Map and directions
Conference address :
Hilton Irvine/Orange County Airport
18800 MacArthur Blvd
Irvine
United States
Map and directions

Further information

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Details

Quality Management and Quality Audit According to GxP/GMP Requirements Hospital - Management
gxp, gmp, quality management, quality audit, fda, qms, quality management system, gmp audit
Professionals, Quality Assurance Documentation Managers Records Managers Document Control Compliance Medical Affairs
10 -- --
English

Other

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