Federal Supply Schedule GS10F0312N

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Attached to: Federal Supply Schedule GS10F0312N Federal contract IDV
Contract number: GS10F0312N
Issued by: General Services Administration Federal Acquisition Service Management Services Center

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General Services Administration

Federal Supply Service Authorized Federal Supply Schedule Price List

On-line access to contract ordering information, terms and conditions, up-to-date pricing, and the option to create an electronic delivery order are available through GSA Advantage!, a menu-driven database system. The INTERNET address for

GSA Advantage! is: GSAAdvantage.gov

Federal Supply Schedule: 00CORP Professional Services Schedule

(PSS)

Contract # GS-10F-0312N For more information on ordering from Federal Supply Schedules click on the FSS Schedules button at http://www.fss.gsa.gov

Contract Period: April 1, 2003 – March 31, 2018

(Current through Modification #PS-0027, dated 3/8/16.)

AQS Management Systems, Inc.

2167 Northdale Blvd NW Minneapolis, MN 55433

Toll Free: 800-633-2588 Fax: 763-746-0504

Website: www.aqsperformance.com Email: ben@aqsperfromance.com

Contract Administration Source: Ben Ames Business Size: Service Disabled Veteran-Owned Small Business (SDVOSB) http://www.aqsperformance.com/�

AQS Management Systems, Inc. GSA Contract GS-10F-0312N Contract Period: Apr. 1, 2003 – Mar. 31, 2018 2167 Northdale Blvd NW, Minneapolis, MN 55433 Phone: 800-633-2588 Website: www.aqsperformance.com

Table of Contents

Title Page

Customer Information.............................................................................................................. 3-4

Company Background

Description of Consultation Services / Training Services...................................................... 6-25

Price Lists............................................................................................................................ 26-42

Customer Information

1a. Table of Awarded Special Item Numbers (SIN):

SIN 874-1 & 874-1RC: Integrated Consultation Services SIN 874-4 & 874-4RC: Training Services: Instructor Led Training, Web Based Training and

Education Courses, Course Development and Test Administration, Learning Management, Internships

1b. Lowest Price Item:

SIN ITEM RATE

874-1 & 874-1RC: Senior $1,137.00/Day 874-4 & 874-4RC: ½ Day Overview $1,112.50

1c. Hourly Rates: See Below

2. Maximum Order: All SIN’s: $1,000,000.00

3. Minimum Order: $100.00

4. Geographic Coverage (delivery area): Domestic and International

5. Point(s) of Production (city, county, state): Minneapolis, Anoka County, MN

6. Discount From List Price or Statement of Net Price:

Prices shown herein are NET Prices; Basic Discounts have been deducted.

7. Quantity/Volume Discount: None

8. Prompt Payment Terms: Net 30 days

9a. Government Purchase Card Acceptance Below Micro-purchase Threshold: Yes

9b. Government Purchase Card Acceptance Above Micro-purchase Threshold: Yes

10. Foreign Items (list by country of origin): None

11a. Time of Delivery: As negotiated and mutually agreed-to for each individual delivery/task order.

11b. Expedited Delivery: As negotiated and mutually agreed-to for each individual delivery/task order.

11c. Overnight and 2-day Delivery: As negotiated and mutually agreed-to for each individual delivery/task order, pending customer pre-approval of any premium costs for expedited shipping and handling.

11d. Urgent Requirements: AQS Management Systems, Inc., will negotiate with the contracting agency on a case-by-case basis in an attempt to meet accelerated delivery of rush requirements.

12. F.O.B. points: Destination

13a. Ordering Address:

Minneapolis, MN 55433

13b. Ordering Procedures:

For supplies and services, the ordering procedures, information on Blanket Purchase Agreements (BPA’s), are found in Federal Acquisition Regulation (FAR) 8.405-3.

14. Payment Address:

Minneapolis, MN 55433

15. Warranty Provision: Contractors standard commercial warranty

16. Export Packaging Charges (if applicable): Not Applicable.

17. Terms and Conditions of Government Purchase Card Acceptance:

The Government Purchase Card is accepted for purchases of any size. (No additional discounts offered on orders placed using credit card.)

18. Terms and conditions of rental, maintenance, and repair (if applicable):

Not Applicable.

19. Terms and conditions of installation, (if applicable): Not Applicable

20. Terms and conditions of repair parts (if applicable): Not Applicable.

20a. Terms and conditions for any other services (if applicable): Not Applicable

21. List of service and distribution points (if applicable): Not Applicable

22. List of participating dealers (if applicable): Not Applicable

23. Preventive maintenance (if applicable): Not Applicable

24a. Special Environmental Attributes: None

24b. Section 508 Compliance: Not Applicable

25. DUNS Number: 808299606

26. System for Award Management (SAM) Completed: Yes

Company Background

AQS Management Systems, Inc. provides consulting, training, coaching, and project assistance in support of organizational improvement and implementation of international management system standards.

We successfully participated in the RAB pilot project for ISO 9000 Lead Auditor Training in 1993 and the ISO 14001 Lead Auditor Training in 1996. No organization has been doing RAB/RABQSA/Exemplar Global Certified Lead Auditor Training longer than AQS Management Systems.

Established in 1989, we have grown to offer a full range of innovative training and project support services to industry, government, non-profit, and service in areas of Quality, Environment, Food Safety, Energy Management, Contingency Planning and Occupational Health and Safety. Our full time staff and regional technical experts are fully qualified to provide the support you need. We have never had a client who failed an audit where we provided direct consulting support.

Our Qualifications The AQS skill set includes trainers and project support personnel with technical expertise in:

Manufacturing Waste Water Treatment

Automotive Service

Health Care Air Pollution

Food Government Aerospace

HACCP

Occupational Health and Safety

Agribusiness

DOD

Contingency Planning

Surface Water Hazard Analysis Medical Device

Resource Management

What We Do Our primary focus is to provide timely, cost-effective advice and support to organizations who intend to use their completed management system to generate profit and reduce risks and costs for their organization. In addition to achieving successful registration, we work with our clients to achieve improved customer satisfaction, improved internal performance, and efficient operations.

A Unique Approach to Project Support AQS’s time-tested approach is truly unique in our industry. Unlike many consulting organizations that work to fit an organization into ISO, we will help you and your team to integrate ISO into your organization. This approach ensures that you have only one system to manage; your business. With the help of our experienced personnel you will never have to manage ISO as a separate set of requirements that fall outside your business processes.

While most ISO experts understand the “rules,” and many of the best understand how to successfully apply the “rules,” AQS Management Systems distinguishes its projects by adding one critical component: we understand when the “rules” apply. Our no-nonsense approach to project support achieves registration and performance results with an emphasis on eliminating unnecessary paperwork and cumbersome rules.

Description of Services

SIN 874-1 & 874-1RC: Integrated Consultation Services

PARTNER –

Functional Responsibility:

Partner level staff will lead projects consisting of Management Systems Implementation, Full System Audits and Consulting in the areas of QMS, EMS, OHS and PS-Prep. They will be the Lead contact for these projects as well as training events.

Education/Experience:

Master's Degree and 14 years experience Bachelor's Degree and 16 years experience High School Diploma and 20 years experience

Training or Certification Requirements: None

SENIOR –

Functional Responsibility:

Senior level staff will assist in projects consisting of Management Systems Implementation, Full System Audits and Consulting in the areas of QMS, EMS, OHS and PS-Prep. They will assist on these projects as well as leading training events. .

Education/Experience:

Master's Degree and 4 years experience Bachelor's Degree and 6 years experience High School Diploma and 10 years experience

MD/TS –

Functional Responsibility:

Medical Device (MD) /Technical Specification (TS) staff will lead projects consisting of Management Systems Implementation, Full System Audits and Consulting in the areas of ISO 13485, TS 16949, ISO 29001. They will be the Lead contact for these projects as well as training events.

MD- Medical Device standard (ISO 13485) TS- Technical Specification standard (TS 16949 or TS 29001)

Education/Experience:

Master's Degree and 4 years experience

AS -

Functional Responsibility:

Aerospace (AS) staff will lead projects consisting of Management Systems Implementation, Full System Audits and Consulting in the areas of AS9100, AS9110 & AS9120. They will be the Lead contact for these projects as well as training events.

AS9100, AS9110 & AS9120 are management systems standards used by Aerospace Manufacturers, Aerospace Maintenance and Aerospace Stockist Distributor users.

Food Safety - Functional Responsibility:

Food Safety staff will lead projects consisting of Management Systems Implementation, Full System Audits and Consulting in the areas of ISO 22000 & FSSC 22000. They will be the Lead contact for these projects as well as training events.

FS- Food Safety Industry standard (ISO 22000 or FSSC 22000) ISO 2000 & FSSC 22000 are management systems standards that deal specifically with food safety in the manufacture of food products.

Service Contract Act:

The Service Contract Act (SCA) is applicable to this contract as it applies to the entire MOBIS Schedule and all services provided. While no specific labor categories have been identified as being subject to SCA due to exemptions for professional employees (FAR 22.1101, 22.1102 and 29 CRF 541.300), this contract still maintains the provisions and protections for SCA eligible labor categories.

If and / or when the contractor adds SCA labor categories / employees to the contract through the modification process, the contractor must inform the Contracting Officer and establish a SCA matrix identifying the GSA labor category titles, the occupational code, SCA labor category titles and the applicable WD number. Failure to do so may result in cancellation of the contract.

SIN 874-4 & 874-4RC: Training Services: Instructor Led Training, Web Based Training and Education Courses, Course Development and Test

AQS Management Systems, Inc. provides consulting, Training (Instructor led and Blended Web and Instructor led), coaching and project assistance in support of organization improvement and implementation of international management standards.

½ Day and 1 Day Overview – QMS/EMS/OHSAS

Who Should Attend:

Those responsible for Quality Management System (QMS) / Environmental Management System (EMS) / Occupational Health and Safety Assessment System (OHSAS) project team members, members of management, senior executives, Quality/Environmental/Health and Safety Assurance Managers, internal auditors, Quality/Environmental/Health and Safety assurance professionals, and anyone who wants an introductory understanding of QMS/EMS/OHSAS.

Course Objectives: To provide decision-makers with information that will help them to provide direction for their existing or planned QMS/EMS/OHSAS quality management system.

Participants will understand:

The requirements of QMS/EMS/OHSAS The ISO process approach and its impact on the organization and the bottom line Understand the implications and benefits for your organization How to ensure benefits and results Managements role in effective internal audits

Training Method: Instructor Led

Additional Instructors Required / Additional Fee: None

½ Day and 1 Day Overview – Ind Sp/Int

Who Should Attend:

Those responsible for Industry Specific (IS) and Integrated Auditor (Int) functions relating to ISO 13485/TS 16949/TS 29001 project team members, members of management, senior executives, Quality/Environmental/Health and Safety Assurance Managers, internal auditors, Quality/Environmental/Health and Safety assurance professionals, and anyone who wants an introductory understanding of ISO 13485/TS 16949/TS 29001.

Course Objectives:

To provide decision-makers with information that will help them to provide direction for their existing or planned ISO 13485/TS 16949/TS 29001 quality management system.

Participants will understand:

The requirements of ISO 13485/TS 16949/TS 29001 The ISO process approach and its impact on the organization and the bottom line Understand the implications and benefits for your organization

½ Day and 1 Day Overview – AS

Those responsible for Aerospace (AS) functions relating to AS9100.AS9110/AS9120 project team members, members of management, senior executives, Quality/Environmental/Health and Safety Assurance Managers, internal auditors, Quality/Environmental/Health and Safety assurance professionals, and anyone who wants an introductory understanding of AS9100.AS9110/AS92120.

To provide decision-makers with information that will help them to provide direction for their existing or planned AS9100.AS9110/AS92120 quality management system.

Participants will understand:

The requirements of AS9100.AS9110/AS92120.

The ISO process approach and its impact on the organization and the bottom line Understand the implications and benefits for your organization

½ Day and 1 Day Overview – FS/Lab

Those responsible for Food Safety (FS) and Laboratory (Lab) functions relating to ISO 22000/FSSC 22000/ISO 17025 project team members, members of management, senior executives, Quality/Environmental/Health and Safety Assurance Managers, internal auditors, Quality/Environmental/Health and Safety assurance professionals, and anyone who wants an introductory understanding of ISO 22000/FSSC 22000/ISO 17025.

To provide decision-makers with information that will help them to provide direction for their existing or planned ISO 22000/FSSC 22000/ISO 17025 quality management system.

Participants will understand:

The requirements of ISO 22000/FSSC 22000/ISO 17025 The ISO process approach and its impact on the organization and the bottom line Understand the implications and benefits for your organization

2 Day - Internal Auditor Training – QMS/EMS/OHSAS

Those responsible for planning and scheduling an audit program for Quality Management System (QMS) / Environmental Management System (EMS) / Occupational Health and Safety Assessment System (OHSAS) and those who must perform audits to QMS/EMS/OHSAS, QMS/EMS/OHSAS Managers, QMS/EMS/OHSAS professionals, ISO Project Managers, ISO Project Team Members or anyone desiring an in-depth understanding of the QMS/EMS/OHSAS Audit Process.

Fully understand and successfully interpret the ISO 9001:2008 requirements Understand how to audit using the process approach Ask audit questions that get results Identify and document nonconformities Audit to the QMS/EMS/OHSAS Quality Management Systems Qualify additional staff to conduct internal audits Provide critical knowledge for your management staff Gain insight into the QMS/EMS/OHSAS audit requirements to augment/sustain your existing program Gain knowledge to help manage a successful QMS/EMS/OHSAS implementation project Provide professional credentials to your internal auditors Conduct an audit against the newly published ISO 19011 Audit Standard Provide critical knowledge for your staff and management

2 Day - Internal Auditor Training – Ind Sp/Int

Those responsible for Industry Specific (IS) and Integrated Auditor (Int) functions relating to planning and scheduling an audit program for ISO 13485/TS 16949/TS 29001and those who must perform audits to ISO 13485/TS 16949/TS 29001, ISO 13485/TS 16949/TS 29001 Managers, ISO 13485/TS 16949/TS 29001 professionals, ISO Project Managers, ISO Project Team Members or anyone desiring an in-depth understanding of the ISO 13485/TS 16949/TS 29001Audit Process

Course Objectives:

Fully understand and successfully interpret the ISO 13485/TS 16949/TS 29001 requirements Understand how to audit using the process approach Ask audit questions that get results Identify and document nonconformities Audit to the ISO 13485/TS 16949/TS 29001 Quality Management Systems Qualify additional staff to conduct internal audits Provide critical knowledge for your management staff Gain insight into the ISO 13485/TS 16949/TS 29001 audit requirements to augment/sustain your existing program Gain knowledge to help manage a successful ISO 13485/TS 16949/TS 29001 implementation project Provide professional credentials to your internal auditors

2 Day - Internal Auditor Training – AS

Those responsible for Aerospace (AS) functions relating to planning and scheduling an audit program for AS9100/AS9110/AS9120 and those who must perform audits to AS9100/AS9110/AS9120, AS9100/AS9110/AS9120 Managers, QMS/EMS/OHSAS professionals, AS Project Managers, ISO Project Team Members or anyone desiring an in-depth understanding of the AS9100/AS9110/AS9120 Audit Process.

Fully understand and successfully interpret the AS9100/AS9110/AS9120 requirements Understand how to audit using the process approach Ask audit questions that get results Identify and document nonconformities Audit to the AS9100/AS9110/AS9120 Quality Management Systems Qualify additional staff to conduct internal audits Provide critical knowledge for your management staff Gain insight into the AS9100/AS9110/AS9120 audit requirements to augment/sustain your existing program Gain knowledge to help manage a successful AS9100/AS9110/AS9120 implementation project Provide professional credentials to your internal auditors

2 Day - Internal Auditor Training – FS/Lab

Those responsible for Food Safety (FS) and Laboratory (Lab) functions relating to planning and scheduling an audit program for ISO 22000/FSSC 22000/ISO 17025 and those who must perform audits to for ISO 22000/FSSC 22000/ISO 17025, for ISO 22000/FSSC 22000/ISO 17025 Managers, for ISO 22000/FSSC 22000/ISO 17025 professionals, ISO Project Managers, ISO Project Team Members or anyone desiring an in-depth understanding of the for ISO 22000/FSSC 22000/ISO 17025 Audit Process

Course Objectives:

Fully understand and successfully interpret the ISO 9001:2008 requirements Understand how to audit using the process approach Ask audit questions that get results Identify and document nonconformities Audit to the for ISO 22000/FSSC 22000/ISO 17025 Quality Management Systems Qualify additional staff to conduct internal audits Provide critical knowledge for your management staff Gain insight into the for ISO 22000/FSSC 22000/ISO 17025 audit requirements to augment/sustain your existing program Gain knowledge to help manage a successful for ISO 22000/FSSC 22000/ISO 17025 implementation project

Provide professional credentials to your internal auditors

2 Day - Blended – QMS/EMS

Those responsible for planning and scheduling an audit program for Quality Management System (QMS) / Environmental Management System (EMS) and those who must perform audits to QMS/EMS, QMS/EMS Managers, QMS/EMS professionals, ISO Project Managers, ISO Project Team Members or anyone desiring an in-depth understanding of the QMS/EMS Audit Process.

Fully understand and successfully interpret the QMS/EMS requirements Audit to the ISO 9001 or SO 14001 Management System Standard Plan, manage, and schedule an audit program Develop a cost-effective and compliant audit system Qualify additional staff to conduct internal audits Provide critical knowledge for your staff and management Gain insight into the QMS/EMS audit requirements to augment/sustain your existing program Gain knowledge to help manage a successful ISO implementation project Document and define your quality system, Implement, design and complete a successful

QMS/EMS project Understand how to audit using the Process Approach Review documents in light of the decreased emphasis on documentation Ask audit questions that get results Identify and document nonconformities

Training Method: Web based and Instructor Led

Additional Instructors Required / Additional Fee: Additional instructor required for students 11-20.

Additional fee for 2nd instructor at student 11 is $1300.

2 Day – Blended – Ind Sp/Int

Those responsible Industry Specific (IS) and Integrated Auditor (Int) functions relating to planning and scheduling an audit program for QMS/EMS and those who must perform audits to QMS/EMS, QMS/EMS Managers, QMS/EMS professionals, ISO Project Managers, ISO Project Team Members or anyone desiring an in-depth understanding of the QMS/EMS Audit Process.

Fully understand and successfully interpret the QMS/EMS requirements Audit to the ISO 13485/TS 16949 or ISO 14001 Management System Standard Plan, manage, and schedule an audit program Develop a cost-effective and compliant audit system Qualify additional staff to conduct internal audits Provide critical knowledge for your staff and management Gain insight into the QMS/EMS audit requirements to augment/sustain your existing program

Gain knowledge to help manage a successful ISO implementation project Document and define your quality system, Implement, design and complete a successful

QMS/EMS project Understand how to audit using the Process Approach Review documents in light of the decreased emphasis on documentation Ask audit questions that get results

Training Method: Web based and Instructor Led

Additional fee for 2nd instructor at student 11 is $1300.

3 Day - Internal Auditor Training – QMS/EMS/OHSAS

Those responsible for planning and scheduling an audit program for Quality Management System (QMS) / Environmental Management System (EMS) / Occupational Health and Safety Assessment System (OHSAS), and those who must perform audits to QMS/EMS/OHSAS, QMS/EMS/OHSAS Managers, QMS/EMS/OHSAS professionals, ISO Project Managers, ISO Project Team Members or anyone desiring an in-depth understanding of the QMS/EMS/OHSAS Audit Process

Course Objectives:

Fully understand and successfully interpret the requirements Understand how to audit using the process approach Ask audit questions that get results Identify and document nonconformities Audit to the QMS/EMS/OHSAS Quality Management Systems Qualify additional staff to conduct internal audits Provide critical knowledge for your management staff Gain insight into the QMS/EMS/OHSAS audit requirements to augment/sustain your existing program Gain knowledge to help manage a successful QMS/EMS/OHSAS implementation project Provide professional credentials to your internal auditors

3 Day - Internal Auditor Training – Ind Sp/Int

Those responsible for Industry Specific (IS) and Integrated Auditor (Int) functions relating to planning and scheduling an audit program for ISO 13485/TS 16949/TS 29001 and those who must perform audits to ISO 13485/TS 16949/TS 29001 Managers, ISO 13485/TS 16949/TS 29001 professionals, ISO Project Managers, ISO Project Team Members or anyone desiring an in-depth understanding of the ISO 13485/TS 16949/TS 29001 Audit Process.

Course Objectives:

Fully understand and successfully interpret the requirements Understand how to audit using the process approach Ask audit questions that get results Identify and document nonconformities Audit to the ISO 13485/TS 16949/TS 29001 Quality Management Systems Qualify additional staff to conduct internal audits Provide critical knowledge for your management staff Gain insight into the ISO 13485/TS 16949/TS 29001 audit requirements to augment/sustain your existing program Gain knowledge to help manage a successful ISO 13485/TS 16949/TS 29001 implementation project Provide professional credentials to your internal auditors

3 Day - Internal Auditor Training – AS

Those responsible in Aerospace (AS) for planning and scheduling an audit program for AS9100/AS9110/AS9120 and those who must perform audits to AS9100/AS9110/AS9120 Managers, AS9100/AS9110/AS9120 professionals, ISO Project Managers, ISO Project Team Members or anyone desiring an in-depth understanding of the AS9100/AS9110/AS9120 Audit Process.

Course Objectives:

Fully understand and successfully interpret the requirements Understand how to audit using the process approach Ask audit questions that get results Identify and document nonconformities Audit to the AS9100/AS9110/AS9120 Quality Management Systems Qualify additional staff to conduct internal audits Provide critical knowledge for your management staff Gain insight into the AS9100/AS9110/AS9120 audit requirements to augment/sustain your existing program Gain knowledge to help manage a successful AS9100/AS9110/AS9120 implementation project Provide professional credentials to your internal auditors

3 Day - Internal Auditor Training – FS/Lab

Those responsible for Food Safety (FS) and Laboratory (Lab) functions relating to planning and scheduling an audit program for ISO 22000/FSSC 22000/ISO 17025 and those who must perform audits to ISO 22000/FSSC 22000/ISO 17025 Managers, ISO 22000/FSSC 22000/ISO 17025 professionals, ISO Project Managers, ISO Project Team Members or anyone desiring an in-depth understanding of the ISO 22000/FSSC 22000/ISO 17025 Audit Process.

Course Objectives:

Fully understand and successfully interpret the requirements Understand how to audit using the process approach Ask audit questions that get results Identify and document nonconformities Audit to the ISO 22000/FSSC 22000/ISO 17025 Quality Management Systems Qualify additional staff to conduct internal audits Provide critical knowledge for your management staff Gain insight into the ISO 22000/FSSC 22000/ISO 17025 audit requirements to augment/sustain your existing program Gain knowledge to help manage a successful ISO 22000/FSSC 22000/ISO 17025 implementation project Provide professional credentials to your internal auditors

4 Day - Integrated – QMS/EMS/OHSAS

Those responsible for Quality Management System (QMS) / Environmental Management System (EMS) / Occupational Health and Safety Assessment System (OHSAS) for planning and scheduling an audit program for ISO 9001, ISO 14001 and/or OHSAS 18001 and those who must perform audits to ISO 9001ISO 14001 and/or OHSAS 18001, QMS/EMS/OHSAS Assurance Managers, Quality/Environmental/Health and Safety professionals, ISO Project Managers, ISO Project Team Members or anyone desiring an in-depth understanding of the ISO 9001/ISO 14001/OHSAS 18001 Audit Process.

Understand and implement the planning required to integrate audit activities across multiple management systems Understand and successfully interpret the requirements of ISO 9001, ISO 14001 and

OHSAS 18001

Plan and conduct Integrated Audits using ISO 19011 Generate documents and records associated with a successful Integrated Audit Use of effective opening and closing meetings to manage the communication process during Integrated Audits Conduct Integrated Audit interviews that generate audit evidence Ensure nonconformities are resolved prior to closing each audit cycle

Intended learning outcomes—students will:

1. Given ISO 9001, ISO 14001 and/or OHSAS 18001 requirements, interpret the requirements of the standard.

2. Given an audit scenario, collect audit evidence appropriate for ISO 9001, ISO 14001, and/or ISO 18001 requirements.

3. Given an audit scenario, write nonconformity statement(s) and document the related audit evidence and requirements that support that nonconformity statement.

4. Understand terms and definitions related to management systems and auditing, including ISO 9001, ISO 14001 &/or OHSAS 18001.

5. Based on ISO 19011, identify the knowledge and skills required for auditors.

6. Based on ISO 19011, identify principles of auditing.

7. Based on ISO 19011, define and describe the roles and responsibilities of the Auditor and the

Audit Team Leader.

8. Based on ISO 19011, describe the personal behaviors of a successful Auditor.

9. Based on ISO 19011, describe the components of the Audit Cycle.

10. Given ISO 9001, ISO 14001 and/or OHSAS 18001 requirements, determine the requirements of the standard where an opportunity exists for integration and describe how these requirements would be audited in an integrated audit.

11. Given ISO 9001, ISO 14001 and/or OHSAS 18001 requirements, as well as company specific requirements, conduct an audit based on the ISO 19011 Audit Cycle including:

Developing and using an integrated audit checklist;

Conducting an opening meeting;

Conducting audit interviews;

Collecting audit evidence and documenting conformities and nonconformities during an audit interview;

Writing an audit report; and Conducting the closing meeting.

Additional benefits associated with attending this course:

Qualify additional staff to conduct audits Provide critical knowledge for your management staff Gain insight into the ISO 9001, ISO 14001 and OHSAS audit requirements to augment/sustain your existing program

Additional Instructors Required / Additional Fee: Additional instructor required for students 19-30.

Additional fee for 2nd instructor at student 19 is $2600.00.

4 Day - Integrated – MD/TS

Those responsible for Medical Device (MD) / Technical Specification (TS) functions relating to planning and scheduling an audit program for ISO 13485/TS 16949/TS 29001, ISO 14001 and/or OHSAS 18001 and those who must perform audits to ISO 13485/TS 16949/TS 29001, ISO 14001 and/or OHSAS 18001, QMS/EMS/OHSAS Assurance Managers, Quality/Environmental/Health and Safety professionals, ISO Project Managers, ISO Project Team Members or anyone desiring an in-depth understanding of the ISO 13485/TS 16949/TS 29001/ISO 14001/OHSAS 18001 Audit Process.

Those who successfully complete this course will:

Understand and implement the planning required to integrate audit activities across multiple management systems

Understand and successfully interpret the requirements of ISO 13485/TS 16949/TS 29001, ISO 14001 and OHSAS 18001

Plan and conduct Integrated Audits using ISO 19011 Generate documents and records associated with a successful Integrated Audit

Use of effective opening and closing meetings to manage the communication process during Integrated Audits

Conduct Integrated Audit interviews that generate audit evidence Ensure nonconformities are resolved prior to closing each audit cycle

Intended learning outcomes—students will:

1. Given ISO 13485/TS 16949/TS 29001ISO 14001 and/or OHSAS 18001 requirements, interpret the requirements of the standard.

2. Given an audit scenario, collect audit evidence appropriate for ISO 9001 (or industry specific QMS standard), ISO 14001, and/or ISO 18001 requirements.

3. Given an audit scenario, write nonconformity statement(s) and document the related audit evidence and requirements that support that nonconformity statement.

4. Understand terms and definitions related to management systems and auditing, including ISO 13485/TS 16949/TS 29001, ISO 14001 &/or OHSAS 18001.

5. Based on ISO 19011, identify the knowledge and skills required for auditors.

6. Based on ISO 19011, identify principles of auditing.

7. Based on ISO 19011, define and describe the roles and responsibilities of the Auditor and the Audit Team Leader.

8. Based on ISO 19011, describe the personal behaviors of a successful Auditor.

9. Based on ISO 19011, describe the components of the Audit Cycle.

10. ISO 13485/TS 16949/TS 29001, ISO 14001 and/or OHSAS 18001 requirements, determine the requirements of the standard where an opportunity exists for integration and describe how these requirements would be audited in an integrated audit.

11. Given ISO 13485/TS 16949/TS 29001, ISO 14001 and/or OHSAS 18001 requirements, as well as company specific requirements, conduct an audit based on the ISO 19011 Audit Cycle including:

Developing and using an integrated audit checklist;

Conducting an opening meeting;

Conducting audit interviews;

Collecting audit evidence and documenting conformities and nonconformities during an audit interview;

Writing an audit report; and Conducting the closing meeting.

Additional benefits associated with attending this course:

Qualify additional staff to conduct audits Provide critical knowledge for your management staff Gain insight into the ISO 13485/TS 16949/TS 29001, ISO 14001 and OHSAS audit requirements to augment/sustain your existing program Understand the intent and purpose of industry specific subject matter such as Core

Tools and 21 CFR 820 where applicable

4 Day – Integrated – AS/FS/Lab

AS9100/AS9110/AS9120/ISO 22000/FSSC 22000/ ISO 17025, ISO 14001 and/or OHSAS 18001, QMS/EMS/OHSAS Assurance Managers, Quality/Environmental/Health and Safety professionals, ISO Project Managers, ISO Project Team Members or anyone desiring an in-depth understanding of the AS9100/AS9110/AS9120/ISO 22000/FSSC 22000/ ISO 17025/ISO 14001/OHSAS 18001 Audit Process multiple management systems

Understand and successfully interpret the requirements of AS9100/AS9110/AS9120/ISO 22000/FSSC 22000/ ISO 17025, ISO 14001 and OHSAS 18001

1. Given AS9100/AS9110/AS9120/ISO 22000/FSSC 22000/ ISO 17025ISO 14001 and/or OHSAS 18001 requirements, interpret the requirements of the standard.

2. Given an audit scenario, collect audit evidence appropriate for ISO 9001 (or industry specific QMS standard), ISO 14001, and/or ISO 18001 requirements.

3. Given an audit scenario, write nonconformity statement(s) and document the related audit evidence and requirements that support that nonconformity statement.

4. Understand terms and definitions related to management systems and auditing, including AS9100/AS9110/AS9120/ISO 22000/FSSC 22000/ ISO 17025, ISO 14001 &/or OHSAS 18001.

5. Based on ISO 19011, identify the knowledge and skills required for auditors.

6. Based on ISO 19011, identify principles of auditing.

7. Based on ISO 19011, define and describe the roles and responsibilities of the Auditor and the

Audit Team Leader.

8. Based on ISO 19011, describe the personal behaviors of a successful Auditor.

9. Based on ISO 19011, describe the components of the Audit Cycle.

10. AS9100/AS9110/AS9120/ISO 22000/FSSC 22000/ ISO 17025, ISO 14001 and/or OHSAS

18001 requirements, determine the requirements of the standard where an opportunity exists for integration and describe how these requirements would be audited in an integrated audit.

11. Given AS9100/AS9110/AS9120/ISO 22000/FSSC 22000/ ISO 17025, ISO 14001 and/or OHSAS 18001 requirements, as well as company specific requirements, conduct an audit based on the ISO 19011 Audit Cycle including:

Developing and using an integrated audit checklist;

Conducting an opening meeting;

Conducting audit interviews;

Collecting audit evidence and documenting conformities and nonconformities during an audit interview;

Provide critical knowledge for your management staff Gain insight into the AS9100/AS9110/AS9120/ISO 22000/FSSC 22000/ ISO 17025, ISO

14001 and OHSAS audit requirements to augment/sustain your existing program

5 Day – Integrated – QMS/EMS/OHSAS

Those responsible for planning and scheduling an audit program for Quality Management System (QMS) / Environmental Management System (EMS) / Occupational Health and Safety Assessment System (OHSAS) related to planning and scheduling an audit program for ISO 9001, ISO 14001 and/or OHSAS 18001 and those who must perform audits to ISO 9001ISO 14001 and/or OHSAS 18001, QMS/EMS/OHSAS Assurance Managers, Quality/Environmental/Health and Safety professionals, ISO Project Managers, ISO Project Team Members or anyone desiring an in-depth understanding of the ISO 9001/ISO 14001/OHSAS 18001 Audit Process.

Understand and implement the planning required to integrate audit activities across multiple management systems Understand and successfully interpret the requirements of ISO 9001, ISO 14001 and OHSAS

18001 Plan and conduct Integrated Audits using ISO 19011 Generate documents and records associated with a successful Integrated Audit Use of effective opening and closing meetings to manage the communication process during

Integrated Audits Conduct Integrated Audit interviews that generate audit evidence Ensure nonconformities are resolved prior to closing each audit cycle

Intended learning outcomes—students will:

1. Given ISO 9001, ISO 14001 and/or OHSAS 18001 requirements, interpret the requirements of the standard.

2. Given an audit scenario, collect audit evidence appropriate for ISO 9001, ISO 14001, and/or

ISO 18001 requirements.

3. Given an audit scenario, write nonconformity statement(s) and document the related audit evidence and requirements that support that nonconformity statement.

4. Understand terms and definitions related to management systems and auditing, including ISO

9001, ISO 14001 &/or OHSAS 18001.

5. Based on ISO 19011, identify the knowledge and skills required for auditors.

6. Based on ISO 19011, identify principles of auditing.

7. Based on ISO 19011, define and describe the roles and responsibilities of the Auditor and the

Audit Team Leader.

8. Based on ISO 19011, describe the personal behaviors of a successful Auditor.

9. Based on ISO 19011, describe the components of the Audit Cycle.

11. Given ISO 9001, ISO 14001 and/or OHSAS 18001 requirements, as well as company specific requirements, conduct an audit based on the ISO 19011 Audit Cycle including:

Developing and using an integrated audit checklist;

Conducting an opening meeting;

Conducting audit interviews;

Collecting audit evidence and documenting conformities and nonconformities during an audit interview;

Additional fee for 2nd instructor at student 19 is $3250.00

5 Day – Integrated – MD/TS

Who should attend:

Understand and successfully interpret the requirements of ISO 13485/TS 16949/TS 29001, ISO 14001 and OHSAS 18001

Intended learning outcomes—students will:

1. Given ISO 13485/TS 16949/TS 29001ISO 14001 and/or OHSAS 18001 requirements, interpret the requirements of the standard.

2. Given an audit scenario, collect audit evidence appropriate for ISO 9001 (or industry specific

QMS standard), ISO 14001, and/or ISO 18001 requirements.

3. Given an audit scenario, write nonconformity statement(s) and document the related audit evidence and requirements that support that nonconformity statement.

4. Understand terms and definitions related to management systems and auditing, including ISO

13485/TS 16949/TS 29001, ISO 14001 &/or OHSAS 18001.

5. Based on ISO 19011, identify the knowledge and skills required for auditors.

6. Based on ISO 19011, identify principles of auditing.

7. Based on ISO 19011, define and describe the roles and responsibilities of the Auditor and the

Audit Team Leader.

8. Based on ISO 19011, describe the personal behaviors of a successful Auditor.

9. Based on ISO 19011, describe the components of the Audit Cycle.

11. Given ISO 13485/TS 16949/TS 29001, ISO 14001 and/or OHSAS 18001 requirements, as well as company specific requirements, conduct an audit based on the ISO 19011 Audit Cycle including:

Developing and using an integrated audit checklist;

Conducting an opening meeting;

Conducting audit interviews;

Collecting audit evidence and documenting conformities and nonconformities during an audit interview;

Provide critical knowledge for your management staff Gain insight into the ISO 13485/TS 16949/TS 29001, ISO 14001 and OHSAS audit requirements to augment/sustain your existing program Understand the intent and purpose of industry specific subject matter such as Core Tools and 21 CFR 820 where applicable

5 Day – Integrated – AS/FS/Lab

Those responsible for Aerospace (AS), Food Safety (FS) and Laboratory (Lab) functions relating to planning and scheduling an audit program AS9100/AS9110/AS9120/ISO 22000/FSSC 22000/ ISO 17025, ISO 14001 and/or OHSAS 18001 and those who must perform audits to AS9100/AS9110/AS9120/ISO 22000/FSSC 22000/ ISO 17025, ISO 14001 and/or OHSAS 18001, QMS/EMS/OHSAS Assurance Managers, Quality/Environmental/Health and Safety professionals, ISO Project Managers, ISO Project Team Members or anyone desiring an in-depth understanding of the AS9100/AS9110/AS9120/ISO 22000/FSSC 22000/ ISO 17025/ISO 14001/OHSAS 18001 Audit Process multiple management systems

Understand and successfully interpret the requirements of AS9100/AS9110/AS9120/ISO 22000/FSSC 22000/ ISO 17025, ISO 14001 and OHSAS 18001

1. Given AS9100/AS9110/AS9120/ISO 22000/FSSC 22000/ ISO 17025ISO 14001 and/or OHSAS 18001 requirements, interpret the requirements of the standard.

2. Given an audit scenario, collect audit evidence appropriate for ISO 9001 (or industry specific QMS standard), ISO 14001, and/or ISO 18001 requirements.

3. Given an audit scenario, write nonconformity statement(s) and document the related audit evidence and requirements that support that nonconformity statement.

4. Understand terms and definitions related to management systems and auditing, including AS9100/AS9110/AS9120/ISO 22000/FSSC 22000/ ISO 17025, ISO 14001 &/or OHSAS 18001.

5. Based on ISO 19011, identify the knowledge and skills required for auditors.

6. Based on ISO 19011, identify principles of auditing.

7. Based on ISO 19011, define and describe the roles and responsibilities of the Auditor and the

Audit Team Leader.

8. Based on ISO 19011, describe the personal behaviors of a successful Auditor.

9. Based on ISO 19011, describe the components of the Audit Cycle.

10. AS9100/AS9110/AS9120/ISO 22000/FSSC 22000/ ISO 17025, ISO 14001 and/or OHSAS

18001 requirements, determine the requirements of the standard where an opportunity exists for integration and describe how these requirements would be audited in an integrated audit.

Developing and using an integrated audit checklist;

Conducting an opening meeting;

Conducting audit interviews;

Collecting audit evidence and documenting conformities and nonconformities during an audit interview;

Provide critical knowledge for your management staff Gain insight into the AS9100/AS9110/AS9120/ISO 22000/FSSC 22000/ ISO 17025, ISO

14001 and OHSAS audit requirements to augment/sustain your existing program

5 Day - Exemplar Global Certified CLA Training – QMS/EMS/OHSAS

Those responsible for planning and scheduling an audit program as a Certified Lead Auditor (CLA) for Quality Management System (QMS) / Environmental Management System (EMS) / Occupational Health and Safety Assessment System (OHSAS) and those who must perform audits to QMS/EMS/OHSAS, QMS/EMS/OHSAS Managers, QMS/EMS/OHSAS professionals, ISO Project Managers, ISO Project Team Members or anyone desiring an in-depth understanding of the QMS/EMS/OHSAS Audit Process

Course Objectives:

Fully understand and successfully interpret the QMS/EMS/OHSAS requirements Audit to the ISO 9001,ISO 14001 or OHSAS 18001 Management System Standard Plan, manage, and schedule an audit program Develop a cost-effective and compliant audit system Qualify additional staff to conduct internal audits Provide critical knowledge for your staff and management Gain insight into the QMS/EMS/OHSAS audit requirements to augment/sustain your existing program Gain knowledge to help manage a successful ISO implementation project Document and define your quality system, Implement, design and complete a successful

QMS/EMS/OHSAS project Understand how to audit using the Process Approach Review documents in light of the decreased emphasis on documentation Ask audit questions that get results

Additional fee for 2nd instructor at student 11 is $2600.00

5 Day – Exemplar Global Certified CLA – Ind Sp/Int

Those responsible for Industry Specific (IS) and Integrated Auditor (Int) functions relating to planning and scheduling an audit program as a Certified Lead Auditor (CLA) for QMS/EMS/OHSAS and those who must…

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File details come from the government source that posted it. Updated Jun 6, 2019.