ComplianceOnline

Good Practices for Data Integrity, the new Guidance and one FDA Inspector's Experience

Instructor: John R Godshalk
Product ID: 704806
Training Level: Intermediate
  • Duration: 60 Min

recorded version

$249.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Mar-2017

Training CD

$349.00
One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days

Customer Care

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Read Frequently Asked Questions

This webinar, by an ex-FDA, will cover Good Data Integrity Practice for GxP environments. Participants will understand what FDA looks for with regard to data integrity, what may need to be audited, the new guidance and application of data integrity, and relevant regulations for data integrity

Why Should You Attend:

In today's strict regulatory environment it is more important than ever for companies and individuals to understand and apply good data integrity practice to comply with FDA regulatory requirements and the new draft guidance.

This session will be presented by R. Godshalk, who served as a Senior Review Biochemical Engineer and Lead cGMP inspector in the Division of Manufacturing and Product Quality at the Center for Biologics Evaluation and Research (CBER), Food and Drug Administration (FDA). Prior to joining FDA he worked as research engineer for 10 years.

Key Learning Objectives:

  • Understand what data integrity is
  • Know the relevant regulations for data integrity
  • Understand why to record data and create records
  • Understand the basics for software and data integrity
  • Know what documentation/evidence does FDA look for during an inspection with regard to data integrity
  • Review the recent draft guidance on data integrity
  • Understand examples of Data Integrity issues: data integrity and the pre-approval inspection, data integrity in the lab, data integrity in the batch record, computer systems, data falsification, importance of audits

Areas Covered in the Webinar:

  • What is data integrity?
  • What are the relevant regulations for data integrity?
  • Why record data and create records?
  • What is the interaction with software and data integrity?
  • What documentation/evidence does FDA look for during an inspection with regard to data integrity?
  • Examples of Data Integrity issues: data integrity and the pre-approval inspection, data integrity in the lab, data integrity in the batch record, computer systems, data falsification, importance of audits
  • Summary/ Q&A

Who Will Benefit:

The following professionals from FDA regulated industries will benefit from this training:

  • Compliance Officers/ Manager
  • Facility Manager
  • Validation Specialists/ Manager
  • Regulatory Affairs Manager
  • Design Team/Architects
  • Quality Manager
  • Documentation specialists
  • Auditors
  • Manufacturing Engineers
Instructor Profile:
John R Godshalk

John R Godshalk
Senior Consultant, Biologics Consulting Group

John R. Godshalk, B.S., MBA, is a Senior Consultant with the Biologics Consulting Group, Inc.

During his tenure at DMPQ, John gained experience with products that include drugs, drug/device combination products, viral and bacterial vaccines, recombinant therapeutic and fractionation products, in vitro diagnostic test kits, and 510K medical devices. His inspection experience includes leading inspections of active pharmaceutical ingredient manufacturers, aseptic filling and finishing facilities, and contract manufacturers. He has performed numerous pre-approval and pre-licensing inspections for biological and biotechnology products. In addition, he has evaluated industry responses both for technical and regulatory merit during FDA regulatory compliance actions, and has assessed these responses and offered alternative solutions to resolve technical issues and regulatory concerns.

John has developed and given training programs for the FDA and regulated industry on pharmaceutical water, processing and instrumentation, lyophilization, cleaning methods and validation, and facilities for cell and gene therapy. He contributed to formulation of FDA policy as a member of the committee writing the Guidance Document for the Facilities and Controls for Cellular and Gene Therapy Product Manufacturing Operations.

John has served as chair in the review of the Chemistry Manufacturing and Controls (CMC) sections of Biologics License Applications and Supplements for both novel and licensed biological products at CBER. He has trained CBER staff on the scientific and regulatory review and evaluation of these applications and supplements.

Prior to joining FDA, John was a research engineer in industrial biotech. He also used his business experience and MBA as a consultant in the areas of business planning, marketing, information technology and strategic planning, financial modeling and analysis, budgeting, business process engineering, project management, and management consulting.

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Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

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