API Spec Q2 provides a new quality management standard for oil and gas service companies. It was created in response to business drivers like increasing well complexity, cost of non-productive time, and the need for consistent risk mitigation. Key aspects of API Spec Q2 include requirements for competency management, risk assessment, contingency planning, supplier controls, and validation of service quality. The standard is intended to improve reliability, minimize risks, and reduce non-productive time during well construction. It also promotes collaboration between service companies and operators to standardize quality expectations across the industry.
ISO 9001-2015 clause 10.2 is different from ISO 9001-2008 corrective action requirements, i tried to capture the updated requirements and with a suggested format for deal with the updated requirements.
ISO/TS 29001:2010 defines the quality management system requirements for the design, development, production, installation and service of products for the petroleum, petrochemical and natural gas industries.
ISO 9001-2015 clause 10.2 is different from ISO 9001-2008 corrective action requirements, i tried to capture the updated requirements and with a suggested format for deal with the updated requirements.
ISO/TS 29001:2010 defines the quality management system requirements for the design, development, production, installation and service of products for the petroleum, petrochemical and natural gas industries.
[Note: This is a partial preview. To download this presentation, visit:
https://www.oeconsulting.com.sg/training-presentations]
ISO 13485:2016 is an international standard that sets out the requirements for a quality management system (QMS) specific to the medical devices industry. The standard focuses on meeting customer and applicable regulatory requirements and is intended for any organization partially or fully involved in the medical device life-cycle.
This presentation can be used to brief your employees, new hires and potential auditees so as to create awareness of the ISO 13485:2016 standard. Alternatively, the presentation may be used to supplement your materials for the training of QA professionals and internal auditors in the medical devices industry.
It covers the what and why of ISO 13485, the QMS key clause structure, the audit approach and also offers practical tips on how to handle an audit session. When you are done teaching this material to your employees, they will be much more informed and comfortable with ISO 13485:2016.
LEARNING OBJECTIVES
1. Provide background knowledge on ISO 13485:2016
2. Gain an overview of ISO 13485:2016 structure and the certification process
3. Understand the audit approach
4. Gather useful tips on handling an audit session
CONTENTS
1. Overview of ISO 13485
About ISO
What are Standards?
Why are Standards Important?
What is ISO 13485?
Who is ISO 13485 For?
What is a Medical Device?
What is a Quality Management System?
How Does ISO 13485 Work?
Benefits that ISO 13485 Will Bring to the Organization
Advantages of Certification
Development of ISO 13485
Why Was ISO 13485 Revised?
Key Improvements to ISO 13485:2016
Relationship of ISO 13485 with ISO 9001
2. ISO 13485:2016 Structure
The ISO 13485:2016 Structure
The Plan-Do-Check-Act (PDCA) Process Model
ISO 13485:2016 Approach is Based on the PDCA Cycle
Documentation Requirements
ISO 13485:2016 Key Clause Structure (4-8)
Clause 4: Quality Management System
Clause 5: Management Responsibility
Clause 6: Resource Management
Clause 7: Product Realization
Clause 8: Measurement, Analysis & Improvement
3. ISO 13485:2016 Certification
Becoming ISO 13485:2016 Certified
ISO 13485:2016 Certification Process
4. Audit Approach
What is a Quality Audit?
What Are Audits Used For?
Types of Quality Audits
Internal Quality Audit
Principles of Auditing
Audit Focus
Audit Approach
Audit Emphasis
Document Review
Audit Findings
5. Handling an Audit Session
Rights of Auditee
Rights of Auditor
How to Handle an Audit Session?
Auditee's Conduct
Interacting with Auditors: Do's
Interacting with Auditors: Don'ts
Agora você pode fazer a certificação internacional, mais aceita no mundo em português no Brasil, seja um inspetor de soldagem internacional. CSWIP 3.1 level 2 welding inspetor
Aproveite esta oportunidade, descontos especiais!!
Agora você pode ser certificado, no que há de melhor no mercado inspeção, CSWIP 3.1 level 2; esta é uma certificação na área de soldagem, onde este profissional pode atuar em vários continentes.
São 4 dias de curso, mais 1 de exame, provas teórica e prática, o curso acontecerá no Rio de Janeiro, de 12 à 16 de abril de 2017.
O número de empresas estrangeiras no Brasil, vai crescer com a abertura da exploração do petróleo, esta é a certificação mais aceita no mercado internacional.
Esteja pronto, não deixe passar a esta oportunidade!!!
André Lima. 21 964143320
The primary objective of ISO 13485 certification is to standardize regulatory requirements for quality management systems. URS provide ISO 13485 certification in all India.
This webinar goes over the major changes of the new ISO 13485:2016 standard, including the upgrade process. Program Manager Rick Burgess presented and responded to questions live on the webinar.
PetroSync - API 580 & API 581 Risk Based Inspection & Base Resource DocumentPetroSync
The course is based on API RP 580 Risk-Based Inspection and API Publication 581, Base Resource Document. The course first explains feasible means and alternatives for achieving a successful RBI program without undue complications. This course deals with RBI framework and methodology in a simple straight forward manner to establish and implement a risk-based inspection program best suited for the company objectives.
Euro tech Providing API-U Approved Specification Q1 9th Ed. Fundamentals Training Course. API-U training is based on the API Specification Q1 9th Edition. This is a fundamental training for understanding the requirement of API-U Specification Q1 9th Ed. log in our site for more info. https://apitrainingcourse.wordpress.com/
[Note: This is a partial preview. To download this presentation, visit:
https://www.oeconsulting.com.sg/training-presentations]
ISO 13485:2016 is an international standard that sets out the requirements for a quality management system (QMS) specific to the medical devices industry. The standard focuses on meeting customer and applicable regulatory requirements and is intended for any organization partially or fully involved in the medical device life-cycle.
This presentation can be used to brief your employees, new hires and potential auditees so as to create awareness of the ISO 13485:2016 standard. Alternatively, the presentation may be used to supplement your materials for the training of QA professionals and internal auditors in the medical devices industry.
It covers the what and why of ISO 13485, the QMS key clause structure, the audit approach and also offers practical tips on how to handle an audit session. When you are done teaching this material to your employees, they will be much more informed and comfortable with ISO 13485:2016.
LEARNING OBJECTIVES
1. Provide background knowledge on ISO 13485:2016
2. Gain an overview of ISO 13485:2016 structure and the certification process
3. Understand the audit approach
4. Gather useful tips on handling an audit session
CONTENTS
1. Overview of ISO 13485
About ISO
What are Standards?
Why are Standards Important?
What is ISO 13485?
Who is ISO 13485 For?
What is a Medical Device?
What is a Quality Management System?
How Does ISO 13485 Work?
Benefits that ISO 13485 Will Bring to the Organization
Advantages of Certification
Development of ISO 13485
Why Was ISO 13485 Revised?
Key Improvements to ISO 13485:2016
Relationship of ISO 13485 with ISO 9001
2. ISO 13485:2016 Structure
The ISO 13485:2016 Structure
The Plan-Do-Check-Act (PDCA) Process Model
ISO 13485:2016 Approach is Based on the PDCA Cycle
Documentation Requirements
ISO 13485:2016 Key Clause Structure (4-8)
Clause 4: Quality Management System
Clause 5: Management Responsibility
Clause 6: Resource Management
Clause 7: Product Realization
Clause 8: Measurement, Analysis & Improvement
3. ISO 13485:2016 Certification
Becoming ISO 13485:2016 Certified
ISO 13485:2016 Certification Process
4. Audit Approach
What is a Quality Audit?
What Are Audits Used For?
Types of Quality Audits
Internal Quality Audit
Principles of Auditing
Audit Focus
Audit Approach
Audit Emphasis
Document Review
Audit Findings
5. Handling an Audit Session
Rights of Auditee
Rights of Auditor
How to Handle an Audit Session?
Auditee's Conduct
Interacting with Auditors: Do's
Interacting with Auditors: Don'ts
Agora você pode fazer a certificação internacional, mais aceita no mundo em português no Brasil, seja um inspetor de soldagem internacional. CSWIP 3.1 level 2 welding inspetor
Aproveite esta oportunidade, descontos especiais!!
Agora você pode ser certificado, no que há de melhor no mercado inspeção, CSWIP 3.1 level 2; esta é uma certificação na área de soldagem, onde este profissional pode atuar em vários continentes.
São 4 dias de curso, mais 1 de exame, provas teórica e prática, o curso acontecerá no Rio de Janeiro, de 12 à 16 de abril de 2017.
O número de empresas estrangeiras no Brasil, vai crescer com a abertura da exploração do petróleo, esta é a certificação mais aceita no mercado internacional.
Esteja pronto, não deixe passar a esta oportunidade!!!
André Lima. 21 964143320
The primary objective of ISO 13485 certification is to standardize regulatory requirements for quality management systems. URS provide ISO 13485 certification in all India.
This webinar goes over the major changes of the new ISO 13485:2016 standard, including the upgrade process. Program Manager Rick Burgess presented and responded to questions live on the webinar.
PetroSync - API 580 & API 581 Risk Based Inspection & Base Resource DocumentPetroSync
The course is based on API RP 580 Risk-Based Inspection and API Publication 581, Base Resource Document. The course first explains feasible means and alternatives for achieving a successful RBI program without undue complications. This course deals with RBI framework and methodology in a simple straight forward manner to establish and implement a risk-based inspection program best suited for the company objectives.
Euro tech Providing API-U Approved Specification Q1 9th Ed. Fundamentals Training Course. API-U training is based on the API Specification Q1 9th Edition. This is a fundamental training for understanding the requirement of API-U Specification Q1 9th Ed. log in our site for more info. https://apitrainingcourse.wordpress.com/
The main differences and challenges between API Q2 and ISO 9001.
Set up in 1997, Environmental and Quality Solutions (EQS) specializes in helping companies streamline and maintain their management systems to achieve ISO standards of Quality, Health & Safety & Environmental Management.
API Spec. Q1 9th. Ed - Lo que hay que saber por Especialistas - En EspañolGestion360
API Spec. Q1 9th Ed, Sistema de Gestion de Calidad para Fabricantes y Proveedores de Servicios Industria de Petroleo y Gas. API Spec. Q1. Quality Oil and Gas Industry
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Critical Facilities Operations Process: Explanations and illustrative examples.
For training videos, please visit https://m.youtube.com/channel/UCYw2fG4p7buyhJD0EYHahuQ
Model Attribute Check Company Auto PropertyCeline George
In Odoo, the multi-company feature allows you to manage multiple companies within a single Odoo database instance. Each company can have its own configurations while still sharing common resources such as products, customers, and suppliers.
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The Roman Empire A Historical Colossus.pdfkaushalkr1407
The Roman Empire, a vast and enduring power, stands as one of history's most remarkable civilizations, leaving an indelible imprint on the world. It emerged from the Roman Republic, transitioning into an imperial powerhouse under the leadership of Augustus Caesar in 27 BCE. This transformation marked the beginning of an era defined by unprecedented territorial expansion, architectural marvels, and profound cultural influence.
The empire's roots lie in the city of Rome, founded, according to legend, by Romulus in 753 BCE. Over centuries, Rome evolved from a small settlement to a formidable republic, characterized by a complex political system with elected officials and checks on power. However, internal strife, class conflicts, and military ambitions paved the way for the end of the Republic. Julius Caesar’s dictatorship and subsequent assassination in 44 BCE created a power vacuum, leading to a civil war. Octavian, later Augustus, emerged victorious, heralding the Roman Empire’s birth.
Under Augustus, the empire experienced the Pax Romana, a 200-year period of relative peace and stability. Augustus reformed the military, established efficient administrative systems, and initiated grand construction projects. The empire's borders expanded, encompassing territories from Britain to Egypt and from Spain to the Euphrates. Roman legions, renowned for their discipline and engineering prowess, secured and maintained these vast territories, building roads, fortifications, and cities that facilitated control and integration.
The Roman Empire’s society was hierarchical, with a rigid class system. At the top were the patricians, wealthy elites who held significant political power. Below them were the plebeians, free citizens with limited political influence, and the vast numbers of slaves who formed the backbone of the economy. The family unit was central, governed by the paterfamilias, the male head who held absolute authority.
Culturally, the Romans were eclectic, absorbing and adapting elements from the civilizations they encountered, particularly the Greeks. Roman art, literature, and philosophy reflected this synthesis, creating a rich cultural tapestry. Latin, the Roman language, became the lingua franca of the Western world, influencing numerous modern languages.
Roman architecture and engineering achievements were monumental. They perfected the arch, vault, and dome, constructing enduring structures like the Colosseum, Pantheon, and aqueducts. These engineering marvels not only showcased Roman ingenuity but also served practical purposes, from public entertainment to water supply.
Synthetic Fiber Construction in lab .pptxPavel ( NSTU)
Synthetic fiber production is a fascinating and complex field that blends chemistry, engineering, and environmental science. By understanding these aspects, students can gain a comprehensive view of synthetic fiber production, its impact on society and the environment, and the potential for future innovations. Synthetic fibers play a crucial role in modern society, impacting various aspects of daily life, industry, and the environment. ynthetic fibers are integral to modern life, offering a range of benefits from cost-effectiveness and versatility to innovative applications and performance characteristics. While they pose environmental challenges, ongoing research and development aim to create more sustainable and eco-friendly alternatives. Understanding the importance of synthetic fibers helps in appreciating their role in the economy, industry, and daily life, while also emphasizing the need for sustainable practices and innovation.
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We all have good and bad thoughts from time to time and situation to situation. We are bombarded daily with spiraling thoughts(both negative and positive) creating all-consuming feel , making us difficult to manage with associated suffering. Good thoughts are like our Mob Signal (Positive thought) amidst noise(negative thought) in the atmosphere. Negative thoughts like noise outweigh positive thoughts. These thoughts often create unwanted confusion, trouble, stress and frustration in our mind as well as chaos in our physical world. Negative thoughts are also known as “distorted thinking”.
1. API SPEC Q2 FOR AUDITING
STANDARDIZATION OF INDUSTRY
EXPECTATIONS FOR OIL AND GAS
Stacey W. Hagen
ExxonMobil Development Company
Drilling Services & Systems Team Lead
API Sub-Committee 18 Chairman - Quality
Bo Creek
Orion Drilling Company
Quality Assurance / Quality Control Manager
2. API SPEC Q2 FOR AUDITING
AGENDA
Objective
– Provide History and Industry Expectations on API Q2
Outline
– Brief History of API
– Business Drivers for New Industry Standard – API Q2
– API Q2 Overview
– Benefits
3. API SPEC Q2 FOR AUDITING
BRIEF HISTORY
API SPEC Q1
4. API SPEC Q2 FOR AUDITING
History of API and Spec Q1
• July 28, 1914 – November 11, 1918
• National Petroleum War Services Committee
• Pooling Program
• 1919 – American Petroleum Institute
• Program was transitioned into a third party audit
program in the mid 1980’s under the Specification
of Quality Programs, API Spec Q1 that is now in its
9th Edition
• Just as there were drivers for the Monogram
Program, one now exists for the certification of
services
5. API SPEC Q2 FOR AUDITING
BUSINESS DRIVERS
FOR API SPEC Q2
6. API SPEC Q2 FOR AUDITING
Absence of a Corporate Management System
Inconsistency in Risk Mitigation
Lack of Implementation
Lack of Oversight
BUSINESS DRIVERS
7. API SPEC Q2 FOR AUDITING
BUSINESS DRIVERS
Increasing complexity of wells
• Need for improved service technology and
equipment / tool reliability
Increasing spread rates on rigs
• Need for systems to ensure uninterrupted
operations
8. API SPEC Q2 FOR AUDITING
BUSINESS DRIVERS
Service centers have more than one
customer
• Additional requirements typically
specified by one or two customers
• A customer may only be 10% of total
business
• Implementation / compliance of
requirements only 10% of the time is
next to impossible
9. API SPEC Q2 FOR AUDITING
BUSINESS DRIVERS - PerceptionThe incident killed 11 workers and
spewed more than 200 million gallons
of crude in what is touted as the
country’s worst oil spill ever.
Subsequently, a moratorium was
imposed on offshore drilling.
10. API SPEC Q2 FOR AUDITING
ROOT CAUSES OF NPT
LACK OF:
Service execution
planning
Personnel
Competency
Lack of or not
Following
procedures
Lack of using history
logs
Contingency
planning
Quality Checks,
Inspection and Test
Preventive Maintenance, Inspection, Test
Programs (PMITP)
12. API SPEC Q2 FOR AUDITING
INDUSTRY RESPONSE
• Realization that ISO 9001 , ISO TS29001 and API
Spec Q1 apply to manufacturing
• API Task Group (TG) 5 developed under API
SC18
• Specification for QMS Requirements for Service
Supply Organizations
• Identify the expectations for execution of
upstream services including well construction,
intervention, production and abandonment
• Published December 15, 2011
13. API SPEC Q2 FOR AUDITING
API SUBCOMMITTEE 18
Life Cycle
Management
API
Spec Q2
API
Spec Q1
Auditor
Effectiveness
Min. Mfg.
Requirements
WeldingMonogram
Program
TG2TG1 TG3 TG4 TG5 TG6 TG7
SC18
CSOEM
15. API SPEC Q2 FOR AUDITING
API SPEC Q2
HOW IS IT DIFFERENT?
16. API SPEC Q2 FOR AUDITING
PROCESS-BASED QMS (ISO 9001, 29001 & API Q1)
17. API SPEC Q2 FOR AUDITING
CUSTOMER
REQUIREMENTS
CUSTOMER
SATISFACTION
INPUT OUTPUT
CONTINUAL
IMPROVEMENT
PROCESS- AND RISK-BASED QMS (API Q2)
18. API SPEC Q2 FOR AUDITING
OVERLAP - API SPEC Q1 VS. API SPEC Q2
General Requirements
Quality Manual
Control of Documents &
Records
Quality Policy
Quality Objectives
Planning
Management Review
Control of Monitoring and
Measurement Equipment
Measurement, Analysis
and Improvement
Training
Corrective and Preventive
Action
19. API SPEC Q2 FOR AUDITING
SERVICE-SPECIFIC Additions - API SPEC Q2
No Claims to Exclusions
Competency of Personnel
Risk Management
Detection Equipment
Service Design
Contingency Planning
Control over Critical Suppliers
Service Quality Plan
Preventive Maintenance, Inspection and
Test
Service Performance Validation
Management of Change
Corrective and Preventive Action
resulting in a change of controls
Customer Notification
Traceability of Critical Services and SRP
20. API SPEC Q2 FOR AUDITING
Elements Requiring Procedures
• Personnel Competency / Training
• Document Control
• Control of Records
• Risk Assessment
• Service Design
• Contingency Planning
• Purchasing
• Verification of Purchased Services &Service
Related Product
• Execution of Service
• Identification & Traceability
• Service Related Product Status
• Customer Property
• Preservation of Service Related Product
• PMIT
• TMMDE
• Service Performance Validation
• Nonconformities
• Management of Change
• Monitoring, Measuring & Improvement
• Internal Audit
• Analysis of Data
• Improvement
• Corrective Action
• Preventative Action
21. API SPEC Q2 FOR AUDITING
1.2 EXCLUSIONS
“When an organization performs activities addressed by this document,
including the provision of service-related product, all requirements shall
be performed and no claims to exclusion of those requirements shall be
permitted.”
Service-related products (SRP): Materials, equipment, and software
used in the execution of a service.
22. API SPEC Q2 FOR AUDITING
COMPETENT
4.3.2 PERSONNEL COMPETENCE
NEW
• Risk Based
• Problem Solving
Competency =
• Education
• Training
• Skills (OJT)
• Experience
23. API SPEC Q2 FOR AUDITING
4.3.2 PERSONNEL COMPETENCE
THE FOUR LEVELS OF LEARNING
Novice
Not
expected
to be able
to perform
Competent
Expected to
perform to
basic
standards
Expert
Creates
knowledge
and teaches
others
Experienced
Beyond
understanding
of what must
be done
24. API SPEC Q2 FOR AUDITING
5.3 RISKS Management
Immediately
1 years
5 years
10 years
25. API SPEC Q2 FOR AUDITING
5.3 RISK MANAGEMENT
Maintain Procedures to controls Risk
throughout Service Execution
• Identify service related risk
• Implement controls
• Notify customer of remaining risk
26. API SPEC Q2 FOR AUDITING
5.4 Design & Development
Every Service includes Design and Development
Planning Inputs Outputs Review Verification Changes
API Q1
Products
Validation
Planning Inputs Outputs Verification Changes
API Q2
Services
Final
Review
Failing to understand what is and is not critical will impact the service design
which will result in increased risks, lack of controls and potential for loss.
27. API SPEC Q2 FOR AUDITING
5.5 CONTINGENCY PLAN
Contingency planning shall be
integrated into services and
supporting processes between
the organization, its suppliers
and the customer”.
28. API SPEC Q2 FOR AUDITING
5.5 CONTINGENCY PLAN
• Actions required
for significant risk
• Assignment of
responsibility &
authority
• Internal and
external
communications
Outputs
Integration
Disruption
Prevention
Mitigation
Measures
Spares
History Risk
Reliability
Contingency
Planning
29. API SPEC Q2 FOR AUDITING
5.6 PURCHASING & CONTROL OF SUPPLIERS
• Determine criticality of the
services and SRP
• Evaluation & Onsite audits
for critical suppliers.
Critical – That deemed by the organization or customer as indispensable or essential,
needed for a stated purpose or task, and requiring specific action
30. API SPEC Q2 FOR AUDITING
5.7.2 SERVICE QUALITY PLAN
Customer Specific for the
Service being performed
Takes into account
Environmental &
Operational Conditions Design and
Development
Personnel
Competence
Contract
Requirements Identification of
Equipment
Risk
Assessment
Contingency
Planning
31. API SPEC Q2 FOR AUDITING
5.7.3 IDENTIFICATION AND TRACEABILITY
• Identification controls must be
put into place to clearly identify
all stages of delivery,
installation, repair
(maintenance), and redress
• Service-related product shall be
identified.
• Critical service-related product
shall be identified and
traceable.
32. API SPEC Q2 FOR AUDITING
5.7.8 PMITP
Is applicable to Service Related Product (SRP)
Equipment Maintenance is handled under Work Environment.
Corrective
Preventive
Predictive• Expensive
• Results in NPT
• Minimizes Corrective
Maintenance
• Focus of API Spec Q2
• SRP Integrity and
Reliability
33. API SPEC Q2 FOR AUDITING
5.7.8 PMITP
Corrective
Preventive
Predictive• Expensive
• Results in NPT
• Minimizes Corrective
Maintenance
• Focus of API Spec Q2
• SRO Integrity and
Reliability
• Reports that document history use, repairs,
modifications, remanufacturing, inspection and test
activities that all direct verification for reuse of
product;
• List of critical spare parts requirements by the
customer and/or technical requirements including
those by the OEM
• Controls that ensure equipment integrity to original
performance requirements and design acceptance
criteria are maintained
• Original performance requirements that cannot be
met shall undergo the MOC process
34. API SPEC Q2 FOR AUDITING
5.7.8 PMITP
• OEM
• Application, use, environments
• PMIT = OEM Recommendations + Owner
of the equipment
35. API SPEC Q2 FOR AUDITING
5.9 SERVICE PERFORMANCE VALIDATION
Validation must be:
• Differs from Validation for
manufactured product
• Validations occur during and
after execution of service(s)
• Carried out in accordance with
Design (5.4), SQP (5.7.2) and
acceptance criteria
36. API SPEC Q2 FOR AUDITING
5.10.4 CUSTOMER NOTIFICATION
• Customers shall be notified:
– When service execution,
does not conform to
requirements
– When SRP does not
conform which has been
delivered or used in the
execution of a service
37. API SPEC Q2 FOR AUDITING
Management
of Change
Process
Execution
Changes
Management
System
Changes
SRP & Design
Changes
Risk
Assessment
Customer
Notification
No
Yes
No
Customer
Accepts?
Higher
Risk?
End of Process
End of Process
Change in
Personnel &
Suppliers
Yes
5.11 Management of Change
38. API SPEC Q2 FOR AUDITING
Impact on Drilling Operations
Resources
-90+ 0 4010 20 160+80
Risk
Assessment
Drilling Operations
Design of
Service
PM
Programs
Contingency
Planning
Maintenance
& Critical Spares
• Assembly
Insp / Test
QA/QC
• Service
Performance
Validation
•BHA Inspections
•MOC
Critical
Suppliers
Time ( rig days)(AFE) Spud
Operations Support
• Well Integrity
Reduction of NPT
Contractor Influence
APISpecQ2
• Tool Insp
@ delivery
Competency
Service
Quality Plans
40. API SPEC Q2 FOR AUDITING
INDUSTRY IMPACT
Operators
Service
Providers
Suppliers
Regulators
and other
Interested
Parties
41. API SPEC Q2 FOR AUDITING
It is not a template that
you fill in and claim
compliance.
It is not a cross
reference between your
management system
and your customer’s.
It is not a manual with
new buzz words that
you present to your
customers.
WHAT API SPEC Q2 IS NOT
42. API SPEC Q2 FOR AUDITING
It is about service quality and risk mitigation supported by
validation and actual service provider performance.
WHAT API SPEC Q2 IS
43. API SPEC Q2 FOR AUDITING
Benefits of Standardization
• Improves service related product reliability
• Minimizes risk through identification, planning & controls
• Identifies critical tasks that impact quality, safety and the
environment
• Minimizes service related risk and improves efficiencies
• Improves communication between service providers and their
suppliers and operators.
44. API SPEC Q2 FOR AUDITING
INDUSTRY
COLLABORATION
45. API SPEC Q2 FOR AUDITING
Industry Collaboration
Beta Test Site Assessments:
• Gaps, hurdles and milestones for auditing to Q2
• Identify competencies / training for API Staff / Auditors
• Identify needed resources
• Types of certifications needed to meet industry needs
• Baker - Completed
• Schlumberger – Completed
• Weatherford – Completed
• Halliburton – Completed
• Orion Drilling – Completed
46. API SPEC Q2 FOR AUDITING
Industry Collaboration
API Spec Q2 Mock Audit:
• Halliburton – Bakersfield, CA
• July 29th – August 2nd 2013
PSL Covered
• Drilling Fluids & Solids
• Cementing
• Completion Tools
• Production Enhancement
• Directional Drilling / MWD / LWD
• Wireline and Perforating
47. API SPEC Q2 FOR AUDITING
Industry Collaboration
API Spec Q2 Reviews:
•Orion Drilling
•Maersk Drilling
•Akita Drilling
•Parker Drilling
•Transocean
•MI Swaco
48. API SPEC Q2 FOR AUDITING
EVOLUTION OF API SPEC Q2
DEVELOPED PUBLISHED BETA TESTING COMPLIANCE CERTIFICATION
API Spec Q2 was
developed in 2010
through 2011.
API Spec Q2 was
published in
December 2011.
A combination of
operators and service
providers participated
in the beta test.
Service providers
start getting their
QMSs in compliance
with API Spec Q2.
Service providers
become certified in
API Spec Q2.
EXPECTATION
Service providers shall
be in compliance in
order to bid on jobs
requiring API Spec Q2.