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Implementation and Management of GMP Data Integrity

Event Details

Implementation and Management of GMP Data Integrity

Time: May 20, 2020 from 10am to 1pm
Location: Online
Street: Online
City/Town: Fremont
Website or Map: https://www.compliance4all.co…
Phone: 8004479407
Event Type: webinar
Organized By: Compliance4all
Latest Activity: Mar 12

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Event Description

Overview:

Data integrity is the assurance that data records are accurate, complete, intact and maintained within their original context, including their relationship to other data records. This definition applies to data recorded in electronic and paper formats or a hybrid of both.

To assure the quality of raw materials, in process materials and finished goods,laboratory data integrity is assuming greater importance in current Good Manufacturing Practices (CGMP) for US Food and Drug Administration (FDA)-regulated industry. Data integrity and security infractions are not only 21 Code of Federal Regulations (CFR) Part 11 issues but also severe CGMP violations.


Why you should Attend: In recent years, FDA has increasingly observed CGMP violations involving data integrity during CGMP inspections. This is troubling because ensuring data integrity is an important component of industry's responsibility to ensure the safety, efficacy, and quality of drugs, biologics and medical devices.

These data integrity-related CGMP violations have led to numerous regulatory actions, including warning letters, import alerts, and consent decrees. Attendees will obtain an understanding of the Regulatory expectations for Data Integrity.

The information provided at the webinar will enable the attendees to review practices at their own site and identify gaps in their own practices.

Areas Covered in the Session:

  • Examples of data integrity pitfalls
  • Part 11 compliance data integrity issues
  • Review of FDA citations related to data integrity

Learning Objectives:
  • Understand the current regulatory position on data integrity
  • Discover the criteria for data integrity
  • Recognize what needs to be addressed to ensure data integrity within a regulated GXP laboratory
  • Learn about approaches to improve data integrity in a laboratory environment
  • Part 11 compliance
  • FDA citations related to data integrity issues

Who Will Benefit:
  • Quality Control Personnel & Management
  • Manufacturing Personnel & Management
  • Senior Management
  • Regulatory Affairs Personnel & Management
  • Quality Assurance Personnel & Management

Speaker Profile
Danielle DeLucy MS, is owner of ASA Training and Consulting, LLC which provides Pharmaceutical and Biologics based companies with training and quality systems assistance in order to meet Regulatory compliance. Prior to this role, Danielle has been in the industry for 17 years serving in numerous Quality Management Roles, such as the Director of Product Quality, the oversight of Sterility Assurance practices and provided QA oversight of numerous filling and packaging operations.

Danielle began her QA career as a Quality Control Pharmaceutical Microbiologist at a contract laboratory where she performed various tests for their clients. In the years after, she has held positions in the Quality management arena while increasing her responsibility.

Event link:

https://www.compliance4all.com/webinar/-502993LIVE?channel=medtechiq-May_2020_SEO

Contact Info

Netzealous LLC, DBA -Compliance4all

Email: support@compliance4All.com

Phone: +1-800-447-9407

Website: https://www.compliance4all.com/

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