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In light of the pandemic situation events until September 2021 are cancelled. We will inform customers directly when the events are rescheduled.    
COVID CANCELLED: Project Management in Human Resources,   Boston MA, Jan 6-8, 2021
COVID CANCELLED: InterDrone, The International Drone Conference,   Cambridge MA, Jan 11-13, 2021
COVID CANCELLED: Supplier Management for Medical Device Manufacturers,   Cambridge MA, Feb 2-4, 2021
COVID CANCELLED: US Immigration Compliance Strategies,   Boston MA, Feb 15-18, 2021
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COVID CANCELLED: Validation, Verification and Transfer of Analytical Methods,   Boston MA, Apr 19-21, 2021
COVID CANCELLED: Computer System Validation - Reduce Costs and Avoid 483s,   Boston MA, May 10-12, 2021
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Following events are tentatively planned but may be rescheduled, based on CDC guidelines or attendee registration interest .    
TENTATIVE: 21 CFR Part 11 Compliance,   Boston MA, Sep 22-24, 2021
TENTATIVE: Quality Control Laboratory Compliance,   Boston MA, Oct 6-8, 2021
TENTATIVE: Analytical Instrument Qualification and System Validation,   Boston MA, Nov 15-17, 2021
TENTATIVE: FDA's New Import Program for 2021,   Boston MA, Dec 7-9, 2021

Boston Professional Events List


60 Minutes Live Webinar Data Security


Date
Oct 12, 2021 - 01:00 PM - Oct 13, 01:00 PM
Organizer
WCS
Venue
online
Location
WCS Consulting Inc.3190 Stirling Rd, Unit K4 ,Hollywood, FL 33021,

Hollywood,
FL,
US,
ZIP: 33021
Phone: 844-267-7299 | 954-947-5671  

Session Highlights
  • GxP/GMP Requirements for Information Technology
  • IT Systems Validation
  • Information Governance
  • Data Security
  • E-Discovery
  • Crisis Preparedness

Overview
There are GMP requirements for information technology. For a drug to be produced in a GxP/GMP compliant manner, some specific information technology practices must be followed. Computer systems involved in the development, manufacture, and sale of regulated product must meet certain requirements.
Data security is the high priority in any organization but especially in a regulated industry.
Companies need to safeguard against every possible vulnerability across their entire infrastructure. In order to successfully safeguard data, data governance needs to be implemented.
Crisis preparedness is the high priority in any organization but especially in a regulated industry.
In this webinar, we will review GMP requirements for IT systems. We will review data security and data governance procedures and how to implement them.
You will also learn how to implement data security, e-discovery and crisis preparedness.


Why one should attend
In the regulated environment which must be GxP/GMP compliant, data integrity is extremely important. Companies need to prevent data breaches from happening.
Data is the key to GMP compliance and ensures traceability of all development, manufacturing, and testing activities. Data provides the route for auditors to assess the overall quality of operations within a company and the final product.
In order to maintain data in GxP/GMP compliant manner, data security procedures should be developed and implemented.
It is imperative to secure data, prepare for e-discovery, and be ready if crisis strikes.
Learn how to secure, manage and govern data as well as IT systems in compliance with GxP/GMP requirements and be able to pass quality audit.
Learn how to ensure that IT systems are in compliance with GxP/GMP requirements and how to prepare for e-discovery and crisis.
key learning objectives
Learn how to secure, manage and govern data as well as IT systems in compliance with GxP/GMP requirements and be able to pass quality audit.
Learn how to ensure that IT systems are in compliance with GxP/GMP requirements and how to prepare for e-discovery and crisis.
Learn how to implement data security, e-discovery and crisis preparedness.


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


Speaker Details


  • Instructor Profile
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.

 Wcs Seminars
Registration Details
(Contact us : 844-267-7299 | 954-947-5671  
Don't wait. Register TODAY or  Email  US [email protected]
 

Event Categories
Keywords: pharmaceutical




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