Previously Recorded Webinars

8/6/2020	ISO 9001:2015 – Introducing the World’s Most Popular Standard
7/28/2020	e-Stewards V.4 Overview
7/20/2020	The R2 V3 – An Early Look
7/16/2020	Statutory and Regulatory Requirements – Expectations in an ISO 9001 QMS Audit
7/2/2020	What to Expect During Your Stage 1 Audit
6/26/2020	e-Stewards V.4 Overview
6/12/2020	ISO 37001:2016 – An Overview
6/4/2020	Non-Applicable Clauses, Permissible Exclusions & Exemptions
5/29/2020	The Interaction of Processes and its Importance to a Successful Audit
5/27/2020	e-Stewards V4 Overview
5/21/2020	ISO 9001:2015 – Knowing What to Expect to Ensure a Stress Free Audit
5/20/2020	Root Cause Analysis & Corrective Action
5/5/2020	ISO 45001 Overview
5/7/2020	Virtual Auditing – Explaining PJR’s Approach and Expectations
5/4/2020	Overview of ISO 27001
4/28/2020	Most Common NCRs in an ISO 13485 Audit
4/16/2020	Top NCRs During ISO 27001 Audits
4/15/2020	What to Expect During Your Stage 1 Audit
4/6/2020	ISO 45001 Overview
4/3/2020	Best Practices for Securely Working Remotely
3/31/2020	Most Common NCRs in an ISO 13485 Audit
3/30/2020	RIOS:2016 Overview
3/26/2020	Virtual Auditing – Explaining PJR’s Approach and Expectations
3/25/2020	Non-Applicable Clauses, Permissible Exclusions & Exemptions
3/18/2020	ISO 27001 – Expectations for Auditing of Annex A Controls
3/11/2020	Statutory and Regulatory Requirements – Expectations in an ISO 9001 QMS Audit
2/13/2020	Root Cause Analysis & Corrective Action
2/7/2020	ISO 9001:2015 – Introducing the World’s Most Popular Standard
2/7/2020	ISO 45001 Overview
1/22/2020	RIOS:2016 Overview
1/15/2020	The Interaction of Processes and its Importance to a Successful Audit
1/10/2020	ISO 45001 Overview
11/27/2019	The R2 V3 Draft – An Early Look
11/27/2019	ISO 37001:2016 – An Overview
11/14/2019	Non Applicable Clauses, Permissible Exclusions & Exemptions
11/14/2019	Risk Assessment & Treatment
10/16/2019	Statutory and Regulatory Requirements – Expectations in an ISO 9001 QMS Audit
10/4/2019	RIOS 2016 Overview
9/4/2019	ISO 9001:2015 – Anticipating Auditor Expectations in Key Areas
8/21/2019	ISO 9001:2015 – Understanding the World’s Most Popular Standard
8/19/2019	The R2 V3 Draft – An Early Look
7/22/2019	e-Stewards V.3 Overview
7/10/2019	What to Expect During Your Stage 1 Audit
7/8/2019	ISO 14001:2015 Lessons Learned
6/24/2019	ISO 45001 – Overview
6/19/2019	The Interaction of Processes and its Importance to a Successful Audit
6/5/2019	Root Cause Analysis & Corrective Action
5/24/2019	ISO 9001:2015 – Introducing the World’s Most Popular Standard
5/15/2019	Non-Applicable Clauses, Permissible Exclusions & Exemptions
4/24/2019	ISO 9001:2015 – Anticipating Auditor Expectations in Key Areas
4/10/2019	Statutory & Regulatory Requirements
4/3/2019	Risk Assessment & Treatment
2/13/2019	Foundations for Planning Your ISMS
1/24/2019	ISO 45001 Overview
1/16/2019	What to Expect During Your Stage 1 Audit
1/8/2019	RIOS:2016 Overview
12/19/2018	Risk Assessment & Treatment
11/8/2018	e-Stewards V.3 Overview
10/2/2018	ISO 45001 – Overview
9/25/2018	RIOS:2016 Overview
9/19/2018	ISO 13485 Overview
9/13/2018	The Interaction of Processes and its Importance to a Successful Audit
8/22/2018	Root Cause Analysis & Corrective Action
7/31/2018	ISO 14001:2015 Lessons Learned
7/27/2018	ISO 27001 Fundamental Concepts
7/25/2018	ISO 13485:2017 Overview
7/11/2018	Statutory & Regulatory Requirements – Expectations in an ISO 9001 QMS Audit
6/27/2018	IATF 16949 Transition Overview
5/23/2018	ISO 14001:2015 Lessons Learned
5/11/2018	ISO 9001:2015 – Approaching Your Transition With Confidence!
4/25/2018	What To Expect During Your Stage 1 Audit
4/10/2018	ISO 45001 Overview
3/21/2018	Risk Assessment & Treatment
3/21/2018	The Interaction of Processes and Its Importance to a Successful Audit
3/9/2018	RIOS:2016 Overview
1/17/2018	ISO 9001:2015 – Approaching Your Transition With Confidence!
12/20/2017	Non-Applicable Clauses, Permissible Exclusions & Exemptions
11/30/2017	What To Expect In Your First PJR Audit
11/8/2017	What to Expect During Your Stage 1 Audit
10/19/2017	Risk Assessment & Treatment Considerations for your ISMS
10/12/2017	ISO 13485:2016 Overview
10/11/2017	ISO 9001:2015 – Approaching Your Transition With Confidence!
9/21/2017	The Interaction of Processes and its Importance to a Successful Audit
9/20/2017	Risk Assessment Considerations For Your ISMS – Part 2
9/6/2017	Statutory & Regulatory Requirements – Expectations in an ISO 9001 QMS Audit
8/10/2017	ISO 9001:2015 – Approaching Your Transition With Confidence!
8/2/2017	IATF 16949 Transition Series Part IV
7/26/2017	IATF 16949 Transition Series Part III
7/25/2017	Non-Applicable Clauses, Permissible Exclusions & Exemptions
7/19/2017	IATF 16949 Transition Series Part II
7/18/2017	What to Expect During Your Stage 1 Audit
7/12/2017	IATF 16949 Transition Series Part I
6/21/2017	ISO 9001:2015 – Approaching Your Transition With Confidence!
5/31/2017	The Interaction of Processes and its Importance to a Successful Audit
5/24/2017	ISO 13485:2016 Overview
5/10/2017	Risk Assessment Considerations For Your ISMS
4/25/2017	ISO 9001:2015 Critical Points of Review During the Transition Audit Process
4/5/2017	ISO 13485:2016 Overview
3/29/2017	IATF 16949 Transition Series Part IV
3/28/2017	What to Expect During Your Stage 1 Audit
3/22/2017	IATF 16949 Transition Series Part III
3/21/2017	ISO/IEC 20000 Overview
3/15/2017	IATF 16949 Transition Series Part II
3/7/2017	IATF 16949 Transition Series Part I
2/23/2017	What’s New in the FSSC 22000 Standard – Version 4:2017?
2/22/2017	R2:2013 Lessons Learned
2/15/2017	Determining the Scope of Your ISMS
2/10/17	AS9100D:2016 Clause-by-Clause Presentation
2/8/17	ISO 9001:2015 – Preparing for a Successful Transition – Newly Updated Following the Successful Publication of ISO 9001:2015
2/3/17	AS9100D:2016 Key Changes
1/4/17	The Interaction of Processes and its Importance to a Successful Audit

CLICK HERE to view PJR previously recorded webinars made before 2017.

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