ComplianceOnline

ISO 9001 and ISO 13485 Upgrades and Impact on the Industry

Instructor: Carmine Jabri
Product ID: 705449
  • Duration: 60 Min
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Read Frequently Asked Questions

This webinar will focus on the recent changes to the ISO 9001 and ISO 13485 quality management system (QMS) standards. Participants will be provided with the tools necessary to help their company plan for the transition to the new editions.

Why Should You Attend:

Companies must upgrade their QMS from ISO 9001:2008 to ISO: 9001:2015 by September 14, 2018 and ISO 13485:2003 to ISO 13485:2016 by February 28, 2019.

This webinar will highlight the major changes to the recent upgrades to ISO 9001 and ISO 13485. The course is designed for staff that is currently working on the transition from 2008 to the 2015 revision of ISO 9001 and/or the 2003 to 2016 transition for ISO 13485. Additionally, this webinar will be helpful for companies who are implementing ISO 9001 and/or 13485 for the first time.

Areas Covered in the Webinar:

  • What the major changes are in the upgraded ISO 9001 and 13485
  • How the ISO 9001: 2015 new format is designed to fit the PDCA cycle
  • Significance of conducting a GAP analysis
  • Impact of the changes on the organization and/or industry
  • How to plan for the inevitable transition to the new editions

Who Will Benefit:

  • Quality Assurance Managers
  • Management Representatives
  • ISO 9001 Implementation Teams
  • Quality System Auditors
  • Regulatory Professionals
  • Manufacturing & Design Engineers
  • Marketing Product Managers
Instructor Profile:
Carmine Jabri

Carmine Jabri
President and CEO, International Consulting Group

Carmine Jabri, PhD, MSJ, MSQM, MHA, is a President and CEO of International Consulting Group, Inc. Dr. Jabri is an experienced Healthcare and Quality Assurance professional with more than twenty years of experience implementing, improving and directing Quality Management Systems and Healthcare Operations.

His career includes expertise in the Biotechnology, Pharmaceuticals, and Medical Device industries. Dr. Jabri's extensive knowledge of regulations and guidelines, coupled with his training and facilitation skills, help him lead the team of E.M.M.A. International consultants to help organizations improve their quality management systems, reduce costs, reduce errors, and comply with federal, state, and international standards and regulations.

Dr. Jabri holds a Doctor of Philosophy in Epidemiology, a Master of Science in Jurisprudence, a Master of Science in Quality Management, a Master of Science in Health Services Administration and a Bachelor of Science in Chemistry.

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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.

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