QA/RA Lead Auditors Course per ISO 13485:2016

Medical devices industry Gsap
Gstudy > Courses and seminars > QA/RA Lead Auditors Course per ISO 13485:2016

Oct 19, 2022

By Adi Azulay, B.Sc., ICQE

1.0

Quality

Audits

Location: Frontal

Starts at: 09:00

Duration: 3 Meetings

Language: English

Gain the confidence to effectively audit a QMS in accordance with internationally recognized best practice techniques.

  • About Adi Azulay, B.Sc., ICQE

    Adi has 6 years experience consulting for and supporting start-up companies in the field of medical devices.She established quality management systems that meet the requirements of ISO13485, ISO9001, MDR and 21 CFR 820 and supported their maintenance. She has experience in trainings for QMS, Technical Writing and Quality culture.In addition, Adi established in regulatory submissions to the European authorities, according...

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We invite you to join in to our Lead Auditors Course

per ISO 13485:2016

Gain the confidence to effectively audit a QMS in accordance with internationally recognized best practice techniques.

Who should attend?

  • Medical Device professionals leading organizational ISO 13485:2016 conformance activities;
  • Anyone with the need to audit an organization’s ISO 13485:2016 QMS.

How will I benefit?

  • Learn how to assess quality management system conformance with ISO 13485:2016 and other applicable standards by understanding how to plan, conduct, and follow up on audits based on the guidelines of ISO 19011:2018;
  • Improve auditing skills.

***Call us about on-site options.

Contact today to book your seat and for more information

Phone: 052-3610566   E-mail:  lital@gsap.co.il

*Call us about on-site options.

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