Our Products
- IATF 16949 Certification
- 5S Awareness Training
- Ppap Documentation Services
- As 9100 Awareness Training
- API Spec Q1 Awareness Training
- IATF 16949 Core Tools Training
- ISO 15378 Awareness Training
- ISO 14001 Awareness Training
- Iso 9001 Awareness Training
- ISO 41001 Awareness Training
- ISO 37001 Awareness Training
- ISO 27001 Awareness Training
- Iso 45001 Awareness Training
- IMS Awareness Training
- IATF 16949 Awareness Training
- ISO 41001 Facility Management System
- 7QC Tools Awareness Training
Industrial Training

Certifications Provided | IATF 16949 |
Target Location | Pan India |
Document verification Mode | Offline |
Training Courses (if applicable) | Food Safety Supervisor Training |
Services offered | Consultancy |
Type of Certification | New Certification |
Type of Industry | All Industry |
Mode of Report | Hard Copy |
IATF 16949 is a global Quality Management System Standard for the Automotive industry. It was developed by the International Automotive Task Force (IATF), with support from AIAG (Automotive Industry Action Group).
The ISO/TS 16949:1999 standard was initially developed in 1999 to harmonize different quality assessment and accreditation methods that give persistent improvement, emphasizing defect prevention and the reduction of variation and waste in the automotive business supply chain. IATF 16949:2016 integrates existing American and European automotive quality management systems standards within the global automotive industry. It aims to eliminate the need for multiple certifications to satisfy multiple customer requirements.
The IATF consists of an international group of vehicle manufacturers i.e. BMW Group, Fiat, Ford Motor Company, General Motors Corporation, PSA Peugeot-Citroen, Renault, Volkswagen and national trade associations – AIAG (America), VDA (Germany), SMMT (UK), ANFIA (Italy) and FIEV (France).
IATF 16949:2016 (replaces ISO/TS 16949:2009) is a standard that builds up the prerequisites for a Quality Management System (QMS), explicitly for the Automotive sector. It applies to any organization which are active in the supply chain of automotive products.It prepares the organization to demonstrate their commitment towards the quality of product and compliance to customer requirements.
PQSmitra has developed a module of IATF 16949 QMS implementation at the client organization. The expertise of past 20 years has supported more than 250 clients from automotive industry to implement simple, practical and effective systems. PQSmitra offers 100% documentation support, training and also the hand holding to team members which makes the entire project execution easy, hassle free and result oriented. The IATF 16949:2016 implementation process is described below:
- Review of the existing Quality Management System in automotive supply chain. This review is carried out by visits.
- Gap analysis and planning for the documentation (Records and Procedures). 100% documentation support is offered by PQSmitra.
- Designing and development of forms, formats and procedures.
- Training and Hand holding/ support for implementation
- Internal audit for verification of implemented system
- Management review
- Certification audit – Stage 1
- Certification audit – Stage 2
- Closure of non-conformities
- Rewarding the certificate to the organization
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Training Duration | Depends upon the Nature of Business, Size & Location |
Course Mode | Offline |
Location | PAN India |
No of people | Will depend on the Nature of Business, Size & Location |
Training Subject | 5s Awareness Training |
Prefered Time slot | Any Preferred Time Slot as per Client |
Course Duration | Depends upon the Nature of Business, Size & Location |
Learning material needed | Will be taken care by PQSmitra |
Training Programme Features
5S is considered as the Foundation of Improvement Activities and its purpose is to involve the workforce in creating a safe, hygienic, satisfying and pleasant work environment. The 5S pillars are Sort (Seiri), Set in Order (Seiton), Shine (Seiso), Standardize (Seiketsu), and Sustain (Shitsuke).
5S describes how to organize a work space for efficiency and effectiveness by identifying and storing the items used, maintaining the area and items, and sustaining the new order. The decision-making process usually comes from a dialogue about standardization, which builds understanding among employees of how they should do the work.
5S Awareness Training Programme introduces participants to 5S& its interpretations. It ensures that all the organizations / personnel understand the fundamental Principles, importance & potential benefits of implementation and challenges of 5S, to provide guidelines for effective implementation.
Who should attend the training?- Management Personnel
- Quality Managers / Executives / Supervisors
- Management Representatives
- Quality Management System Consultant
- Introduction to 5S
- Fundamental Principles of 5S
- Importance and Potential Benefits of 5S
- Challenges of 5S
- Effective Implementation of 5S
- End of Training Programme
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Type Of Service Provider | Individual Consultant |
Project Duration | Depends on Nature of Business, Size & Location |
Mode Of Service | Online |
Company Manpower | 20-50 |
Language | English, Hindi, Marathi, Gujrati and other regional languages |
Type of service | Existing company modification |
Location | Pan India |
Production Part Approval Process (PPAP) is a process, which is standardized in industries such as automotive and aerospace. PPAP documents helps manufacturers & suppliers to communicate and approve production designs & processes for the entire stages of manufacturing cycle i.e before, during and after.
The PPAP process consists of 18 elements, that are required for approval of production level parts. But there are five elements, which are generally accepted for PPAP submission levels. Requirements in regard to PPAP does differ from client to client.
PPAP documents are required as a requirement of IATF 16949 certification, AS 9100 certification etc. and also as a specific requirement from the clients from the Automotive and Aerospace Industry.
Methodology of PPAP Documentation Service by PQSmitraThe PPAP documentation service by PQSmitra is very practical and effective. The sequence of activities are as under:
- Understanding the PPAP documentation requirements.
- Review of the manufacturing process and planning for the documentation
- Preparation of the PPAP documents and submission for review
- Modifications and Finalization of documents.
- Finalization and closure
- Time saving / Cost Saving/ Effectiveness.
- Professional way of documentation
- Documentation accepted by OEMs and client organizations
- Value addition through expertise for more than 20 years
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Training Duration | Depends upon the Nature of Business, Size & Location |
No Of Persons | Will depend on the Nature of Business, Size & Location |
Training Subject | AS 9100 Awareness Training |
Preferred Time Slot | Any Preferred Time Slot as per Client |
Course Mode | offline |
Course duration | Depends upon the Nature of Business, Size & Location |
Learning Materials | Will be taken care by PQSmitra |
Training Programme Features
AS 9100 is an internationally recognized Quality Management System standard, which can be applied / implemented to organizations that design, develop or provide product and services to Aviation, Space and Defense industry, created by International Aerospace Quality Group. The standard provides suppliers with requirements for creating and maintaining a comprehensive quality system for providing safe and reliable products to the ASD industry, as well as civil and military aviation requirements.
This Training Programme introduces participants to AS 9100: 2016 Aerospace Quality Management System Standard, gives an overview of new requirements & its interpretations. The Training Programme is useful for all the organization’s / personnel to understand the focus of AS 9100 and guidance on effective implementation.
Who should attend the training?- Quality Managers / Executives
- Management Representatives
- Consultants
- Personnel wishing to attend AS 9100 Internal or Lead Auditor Training Programme
- Introduction to AS 9100
- Overview of Revision History
- AS 9100 standard requirements
- Quality Management Principles
- Leadership and Planning
- Risk Based Thinking
- Support Processes
- Operations & its Controls
- Performance Evaluation
- Improvement
- End of Training Programme
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API Spec Q1 Awareness Training
Rs 25,000 / ServiceGet Latest Price
Training Duration | Depends upon the Nature of Business, Size & Location |
No Of Persons | Will depend on the Nature of Business, Size & Location |
Training Subject | API Spec Q1 Awareness Training |
Preferred Slot | Any Preferred Time Slot as per Client |
Course Mode | Offline |
Course duration | Depends upon the Nature of Business, Size & Location |
Learning Materials | Will be taken care by PQSmitra |
Training Programme Features
API certification mainly focus on safety requirements particularly in oil and gas industry as requirements are very stringent as a minor deviation in the product / component can lead to a major catastrophe. The product quality and operational consistency are the prime parameters to avoid any safety related issue at the site. API Standards helps to improve the safety of industry tasks, guarantee the quality, help minimize expenses, diminish waste, and limit the confusion in an oil and gas industry.
This Training Programme introduces participants to American Petroleum Institute (API) Standard & gives an overview of new requirements & its interpretations. The Training Programme is useful for all the organizations / personnel to understand the system related requirements in manufacturing the products for oil and gas industry.
Who should attend the training?- Quality Managers / Executives
- Management Representatives
- API Consultants
- Introduction to API
- Overview of API Spec Q1, Q2 and Monogram Programme
- Certification Process
- End of Training Programme
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IATF 16949 Core Tools Training
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Course Mode | Offline |
Training Duration | Any Preferred Time Slot as per Client |
No Of Persons | Will depend on the Nature of Business, Size & Location |
Preferred Time Slot | Any Preferred Time Slot as per Client |
Training Subject | Training Programme Features The training introduces participants to Core Tools of IATF & its interpr |
Course Duration | Depends upon the Nature of Business, Size & Location |
Learning Material Needed | Will be taken care by PQSmitra |
Training Programme Features
The training introduces participants to Core Tools of IATF & its interpretations. The aim of this course is to create awareness on use of Core Tools – APQP, Control Plan, FMEA, MSA, SPC, PPAP and to make the participant understand the requirements of TS 16949:2016 and linkage with below mentioned core tools.
APQP:Advanced Product Quality Planning (APQP) is a product development methodology followed in IATF 16949, TS 16949. The purpose of APQP is “to produce a product quality plan which will support development of a product or service that will satisfy the customer.”
Control Plan:Another standard method of IATF 16949, TS 16949 but extensively used in all industries with same or similar requirements. Control plan defines the controls exercised by the organization on various processes during different stages.
Control plan is applicable at 3 stages mainly
- Prototype development stage
- Pre-launch stage
- Production stage
Both part specific and product family based control plans are used and provide guidance for process and product acceptance to concerned decision makers which may include machine operator, quality personnel or customer.
FMEA:Failure mode and effects analysis (FMEA) is a prevention based early warning system used widely in IATF 16949, Reliability Engineering, Product Development and Operations management. FMEA is a team activity which identifies potential failure modes based on past experience with similar products or processes or based on common failure to prevent such failures in advance and saving potential losses, cost and time.
MSA:Measurement System Analysis (MSA) is a collection of many statistical analysis methods of evaluating variability in the measurement process. Some popular methods of MSA include Gauge R&R analysis, bias Study, Linearity study, measurement uncertainty etc.
The processes that produce a product may vary, the process of obtaining measurements and data may have variation and produce defects. A Measurement Systems Analysis (MSA) evaluates the test method, measuring instruments, and the entire process of obtaining measurements to ensure that variability of measurement system is within acceptable limits and to evaluate its impact on process acceptance indicators.
SPC:SPC (Statistical Process Control) is also a collection of statistical methods used to control a process within desired limits and to identify patterns of normal (random or chance cause) variation and special (assignable cause) variation in order to identify opportunities for intervention in the process and to take correct decision on process and product acceptance.
PPAP:Production Part Approval Process (PPAP) is mechanism of qualifying a process for production during various stages e.g. Prototype development, Pre-launch and routine / bulk production.
In IATF 16949 system, a supplier obtains PPAP approval from customer based on fulfillment of process qualification requirements set by customer or as per PPAP manual where no specific requirements are set by customer.
Who should attend the training- Factory Manager / Head
- Quality Manager / Executive / Supervisor
- Management Representative
- Production &/or Process Design Managers
- Cross Functional Team of Automotive Supply Chain
- ISO /IATF Consultant
- Introduction of IATF 16949 Core Tools
- Advance Part Quality Planning (APQP)
- Process flowchart
- Control plan
- Failure Mode & Effects Analysis (FMEA)
- Measurement System Analysis (MSA)
- Statistical Process Control (SPC)
- Production Part Approval Process (PPAP)
- End of Course
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Preferred Time Slot | Any Preferred Time Slot as per Client |
Training Duration | Depends upon the Nature of Business, Size & Location |
No Of Persons | Depends upon the Nature of Business, Size & Location |
Location/City | Pan India |
Course Mode | Offline |
Training Subject | ISO 15378 Awareness Training |
Course Duration | Depends upon the Nature of Business, Size & Location |
Learning Material Needed | Will be taken care by PQSmitra |
Training Programme Features
ISO 15378:2017 (GMP – Good Manufacturing Practices) is an application standard for the design, manufacture and supply of primary packaging materials for medicinal products.
Good Manufacturing Practice (GMP) is a term that is renowned worldwide for the control and management of manufacturing, testing and final quality control of food / beverage, pharmaceutical goods and their primary packaging. GMP is a set of rules that gives you the affirmation that your item is safe. GMP is responsible for the safety, efficiency and quality of pharmaceutical products, cosmetic products, edible products and their primary packaging.
This Training Programme introduces participants to ISO 15378 and gives an overview of new requirements & its interpretations. The Training Programme is useful for all the organizations / personnel to develop an effective management system with reference to Good Manufacturing Practices (GMP) for Primary Packaging Materials of Medicinal Products.
Who should attend the training?- Quality Managers / Executives
- Management Representatives
- Management System Consultants
- Personnel wishing to attend Internal or Lead Auditor Training Programme
- Introduction to ISO 15378
- Overview of Revision History
- System designating and Planning
- Required Documentation
- Operational Planning & Control
- Performance Evaluation
- Improvement
- End of Training Programme
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Preferred Time Slot | Any Preferred Time Slot as per Client |
Training Duration | Depends upon the Nature of Business, Size & Location |
No Of Persons | Depends upon the Nature of Business, Size & Location |
Course Mode | Offline |
Training Subject | ISO 14001 Awareness Training |
Course Duration | Depends upon the Nature of Business, Size & Location |
Training Programme Features
ISO 14001 is an (EMS) Environmental management system standard. This Training Programme covers discussions on what EMS and its implementation methodology. It offers an overview of ISO 14001 requirements & its interpretations.
ISO 14001 Environmental management system focuses on
- Legal compliances
- Pollution control
- Conservation of resources
The Training Programme is incredibly useful for all the organizations / personnel to understand the main focus points, the benefits and simple implementation methodology for better effectiveness of the system.
Who should attend the training?- Environmental Managers / Executives
- Management Representatives
- EMS Consultants
- Personnel wishing to attend Internal or Lead Auditor Training Programme
- Introduction to ISO 14001
- Overview of Revision History
- Context of Organization
- EMS Planning
- Environmental programmes
- Aspect Identification & Its Assessment
- Risk Based Thinking
- Required Documentation
- Operational Planning & Control
- Performance Evaluation
- Improvement
- End of Course
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Certifications Provided | ISO 9001 |
Target Location | Pan India |
Document verification Mode | Offline |
Training Courses (if applicable) | ISO 9001 Awareness Training/Industrial Training |
Services offered | Consultancy |
Type of Industry | All Industry |
Mode of Report | Hard Copy |
Training Programme Features
ISO 9001 awareness training introduces participants to ISO 9001:2015 & gives an overview of the requirements & its interpretations. ISO 9001 is a generic standard applicable for any organization irrespective of its size, location and nature of operations. It helps to streamline the business processes for better optimization, efficiency and effectiveness
The training is incredibly useful for all the organizations / personnel to understand the focus points of ISO 9001 implementation and its benefits to the overall business management. The training also covers the simple methodology for effective implementation of ISO 9001 – Quality Management System with right spirit keeping the benefits in mind.
Who should attend the training?- Quality Managers / Executives
- Management Representatives
- QMS Consultants
- Personnel wishing to attend Internal or Lead Auditor course
- Introduction to ISO 9001
- Overview of Revision History
- Quality Management Principles
- Context of Organization
- QMS Planning
- Process Approach
- Leadership
- Risk Based Thinking
- Required Documentation
- Operational Planning & Control
- Performance Evaluation
- Improvement
- End of Course
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Preferred Time Slot | Any Preferred Time Slot as per Client |
Training Duration | Depends upon the Nature of Business, Size & Location |
No Of Persons | Depends upon the Nature of Business, Size & Location |
Course Mode | Offline |
Training Subject | ISO 41001 Awareness Training |
Course Duration | Depends upon the Nature of Business, Size & Location |
Learning Material Needed | Will be taken care by PQSmitra |
Training Programme Features
ISO 41001 Facility Management (FM) combines various disciplines in order to control the economies efficiency and productivity of societies, communities and organizations, as well as the manner in which individuals interact with the built environment. FM affects the health, well-being and quality of life of much of the world’s societies and population through the services it manages and delivers.
This Training Programme introduces participants to ISO 41001 and gives an overview of new requirements & its interpretations. The Training Programme is useful for all the organizations / personnel to develop a management system with reference to Facility Management.
Who should attend the training?- Facilities Managers
- Facilities Services Providers
- FM Management System Consultants
- Personnel wishing to attend Internal or Lead Auditor Training Programme
- Introduction & History of ISO 41001
- Facility Management related requirements
- Implementation guidelines
- Required Documentation
- Operational Planning & Control
- Performance Evaluation
- Improvement
- Overview of ISO 41001 Specific Requirements
- End of Training Programme
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Preferred Time Slot | Any Preferred Time Slot as per Client |
Training Duration | Depends upon the Nature of Business, Size & Location |
No Of Persons | Depends upon the Nature of Business, Size & Location |
Location/City | Pan India |
Course Mode | Offline |
Training Subject | ISO 37001 Awareness Training |
Course Duration | Depends upon the Nature of Business, Size & Location |
Learning Material Needed | Will be taken care by PQSmitra |
Training Programme Features
ISO 37001 – Anti-Bribery Management System is an internationally recognized standard which helps organization to fight against the corruption, by establishing the culture of integrity, transparency and compliance. The Anti-Bribery Management System can be used by any organization that is large or small, public or private and in any part of the country. This is the effective tool, which can be adapted according to the organization size, nature and the risk of bribery it faces.
This Training Programme introduces participants to ISO 37001 and gives an overview of new requirements & its interpretations. The Training Programme is useful for all the organizations / personnel to develop a framework for prohibiting, preventing, detecting, reporting and dealing with any bribery that does occur.
Who should attend the training?- Top Management
- HR & Admin Manager
- ABMS Consultants
- Introduction & History of ISO 37001
- Context of Organization
- Requirements of Anti-Bribery Management System
- Risk Based Thinking
- Required Documentation
- Operational Planning & Control
- Performance Evaluation
- Improvement
- Overview of ISO 37001 Specific Requirements
- End of Training Programme
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Preferred Time Slot | Any Preferred Time Slot as per Client |
Training Duration | Depends upon the Nature of Business, Size & Location |
No Of Persons | Depends upon the Nature of Business, Size & Location |
Course Mode | Offline |
Training Subject | ISO 27001 Awareness Training |
Course Duration | Depends upon the Nature of Business, Size & Location |
Learning Material Needed | Will be taken care by PQSmitra |
Training Programme Features
This Training Programme introduces participants to ISO 27001 ISMS (Information Security Management system) requirements and control points. Training offers an overview of new requirements & its interpretations.
ISO 27001:2013 ISMS standard focuses on information security towards CIA (Confidentiality, Integrity and Availability) of the data. Training offers insight on critical points, controls and system implementation methodology in accordance with ISMS statement of applicability.
Training provides guidelines to implement 114 controls of information security perspective. The training on ISMS requirements with respect to individual system domain offer simple and practical methodology for better system implementation and achieve business targets. The Training Programme is useful for all the organization / personnel to develop an effective information security management system.
Who should attend the training?- Management Representatives
- IT Professionals
- ISMS Consultants
- Personnel wishing to attend ISO 27001 ISMS Internal or Lead Auditor Training Programme
- Introduction to ISO 27001
- Overview of Revision History
- Basic requirements of ISO 27001:2013 & its interpretation
- Risk assessment
- SOA
- Overview of implementation & certification
- End of Training Programme
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Preferred Time Slot | Any Preferred Time Slot as per Client |
Training Duration | Depends upon the Nature of Business, Size & Location |
No Of Persons | Depends upon the Nature of Business, Size & Location |
Location/City | Pan India |
Course Mode | Offline |
Training Subject | ISO 45001 Awareness Training |
Course Duration | Depends upon the Nature of Business, Size & Location |
Training Programme Features
This Training Programme introduces participants to ISO 45001:2018 & gives an overview of new requirements & its interpretations. ISO 45001 is an Occupational Health and Safety standard. This Training Programme covers an overview of ISO 14001 requirements, its interpretations and implementation methodology.
ISO 45001 Environmental management system focuses on
- Legal compliances
- Occupational Health related requirements
- Occupational Safety related requirements
- Hazard analysis and Risk assessment
- Planning for Risk mitigation / elimination
The Training Programme is incredibly useful for all the organizations / personnel to understand the focus points, the benefits and simple implementation methodology for better effectiveness of the system.
Who should attend the training?- Safety Officers / Managers / Executives
- Management Representatives
- OHS Consultants
- Personnel wishing to attend Internal or Lead Auditor Training Programme
- Introduction to ISO 45001
- Overview of Revision History
- Summary of Changes in ISO 45001
- Context of Organization & Requirements of Interested Party
- OHS Planning
- Workers Participation and Consultation
- Hazard Identification & Assessment of Risk
- Required Documentation
- Operational Planning & Control
- Outsourcing, procurement & contractor
- Performance Evaluation
- Improvement
- End of Training Programme
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IMS Awareness Training
Rs 25,000 / DayGet Latest Price
Preferred Time Slot | Any Preferred Time Slot as per Client |
Training Duration | Depends upon the Nature of Business, Size & Location |
Number of employee | Depends upon the Nature of Business, Size & Location |
Location / city | PAN India |
Training Subject | IMS (ISO 9001, ISO 14001, ISO 45001) Awareness Training |
Couse Mode | Offline |
Course Duration | Depends upon the Nature of Business, Size & Location |
Training Programme Features
This Training Programme introduces participants to ISO 9001:2015, ISO 14001:2015 & ISO 45001:2018 and gives an overview of new requirements & its interpretations.
The training covers
- Introduction to ISO 9001 Quality management system, its focus points and implementation methodology
- Introduction to ISO 14001 Environmental management system, its focus points and implementation methodology
- Introduction to ISO 45001 Occupational Health and Safety system, its focus points and implementation methodology
The Training Programme is incredibly useful for all the organizations / personnel to understand the terminology, critical points and guidance for better effectiveness of the system.
Who should attend the training?- QHSE Managers / Executives
- Management Representatives
- QMS / EMS / OHSMS Consultants
- Personnel wishing to attend Internal or Lead Auditor Training Programme
- Introduction to ISO 9001, ISO 14001 & ISO 45001
- Overview of Revision History
- P-D-C-A, Process Approach & Benefits of its Implementation
- Context of Organization – QMS / EMS/ OHSMS
- Interpretation of basic requirements of ISO 9001, ISO 14001 & ISO 45001 in regards to
- Context of organization
- Leadership – Consultation & participation of workers
- QMS / EMS / OHSMS Planning
- Risk Based Thinking & Objectives
- Support processes including
- Required Documentation
- Operational planning & control
- Performance evaluation
- Improvement
- End of Training Programme
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Requirement Type | Corporate |
Course Duration | Will depend on the Nature of Business, Size & Location |
Training Subject | IATF 16949 Awareness Training |
Preferred Time Slot | Any Preferred Time Slot as per Client |
Training Duration | Depends upon the Nature of Business, Size & Location |
Number of people | Will depend on the Nature of Business, Size & Location |
Learning Material Needed | Will be taken care by PQSmitra |
Training Programme Features
IATF 16949 is a global Quality Management System Standard for the Automotive industry. It was developed by the International Automotive Task Force (IATF), with support from AIAG (Automotive Industry Action Group).
The ISO/TS 16949:1999 standard was initially developed in 1999 to harmonize different quality assessment and accreditation methods that give persistent improvement, emphasizing defect prevention and the reduction of variation and waste in the automotive business supply chain. IATF 16949:2016 integrates existing American and European automotive quality management systems standards within the global automotive industry. It aims to eliminate the need for multiple certifications to satisfy multiple customer requirements.
This Training Programme introduces participants to IATF 16949:2016 Automotive QMS Standard & gives an overview of new requirements & its interpretations. The Training Programme is useful for all the organizations / personnel to understand the focus of IATF 16949 and salient features, simple and practical implementation methodology.
Who should attend the training- Quality Managers / Executives
- Management Representatives
- QMS / IATF 16949 Consultants
- Personnel wishing to attend IATF 16949:2016 Internal or Lead Auditor Training Programme
- Introduction to IATF 16949
- Salient Features of IATF 16949
- Requirements of IATF 16949:2016
- Focus of IATF 16949
- Introduction to IATF 16949 core tools
- Specific requirements of IATF 16949:2016
- Leadership
- Guidance on effective implementation
- End of Training Programme
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ISO 41001 Facility Management System
Rs 40,000 / CertificateGet Latest Price
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Type of Certification | New Certification |
Type of Industry | All Industry |
Mode of Report | Hard Copy |
Certifications Provided | ISO 14001 |
Target Location | Pan India |
Document verification Mode | Offline |
Training Courses (if applicable) | Depends on the service |
Services offered | Consultancy |
ISO 41001 Facility Management (FM) combines various disciplines in order to control the economies efficiency and productivity of societies, communities and organizations, as well as the manner in which individuals interact with the built environment. FM affects the health, well-being and quality of life of much of the world’s societies and population through the services it manages and delivers.
ISO 410001 is an organizational function which integrates People, Place and Process within the built environment for the purpose of improving the life quality of people and the productivity of the core business.
ISO 41001:2018 was developed for organisations that incorporate or run facilities management systems which have the option of introducing compliance with the new standard into their business.
The main priority of an FM is keeping people alive and safe. Facility managers need to operate at two levels:
- Strategically-tactically: helping clients, customers and end-users understand the potential impact of their decisions on the provision of space, services, cost and business risk.
- Operationally: ensuring corporate and cost effective environment for the occupants to function.
According to the International Facility Management Association (IFMA): FM is the practice of coordinating the physical workplace with the people and work of the organization. It integrates the principles of business administration, architecture and the behavioral and engineering sciences”.
FM covers these two main areas: ‘Space and Infrastructure’ (such as planning, design, workplace, construction, lease, occupancy, maintenance and furniture) and ‘People and Organisation’ (such as catering, cleaning, ICT, HR, accounting, marketing, hospitality). These two broad areas of operation are commonly referred to as “hard FM” and “soft FM”. The first refers to the physical built environment with focus on (work-) space and (building-) infrastructure. The second covers the people and the organization and is related to work psychology and occupational physiology.
The practical and effective system implementation approach is adopted towards ISO 41001 certification at the organization. PQSmitra Team helps in easy understanding of the standard requirements and simple methods for effective compliance. 100% documentation support is offered to achieve successful certification in addition to enhanced operational controls. The implementation process is described below:
- Initial visits and review of the existing system
- Identification of controls and planning for implementation
- Documentation including procedures, work instructions etc.
- Internal audit for verification of implemented system
- Management review
- Certification audit – Stage 1&Stage 2
- Closure of non-conformities
- Rewarding the certificate to the organization
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Training Subject | 7QC Tools Awareness Training |
Preferred Time Slot | Any Preferred Time Slot as per Client |
Training Duration | Depends upon the Nature of Business, Size & Location |
No Of Persons | Will depend on the Nature of Business, Size & Location |
Course Mode | Offline |
Course Duration | Depends upon the Nature of Business, Size & Location |
Learning Material Needed | Will be taken care by PQSmitra |
Training Programme Features
The 7 QC tools are fundamental instruments to improve the process and product quality. They are used to examine the production process, identify the key issues, control fluctuations of product quality and give solutions to avoid future defects. The benefits of 7QC tools can be described as below:
- Improve management decision making skills.
- Collect, present, Identify and analyses data.
- Implement Six Sigma.
- Control cost of poor quality.
- Reduce variations and improve quality.
- Reduce defects and improve production.
- Reduce cycle time and improve efficiency.
This Training Programme introduces participants to 7 QC Tools & its interpretations. It provides all the organizations / personnel with the required knowledge & skills in order to enable them to capture, compile, analyze & interpret the data collected through various sources. On completion of this Training Programme, the participants are able to utilize the gained knowledge for effective utilization of 7 QC tools.
Who should attend the training?- Management Personnel
- Quality Managers / Executives / Supervisors
- Management Representatives
- Quality Management System Consultant
- Introduction to 7 QC Tools.
- Stratification (Divide and Conquer)
- Check Sheet (Tally Sheet)
- Cause-and-effect diagram (“fishbone” or Ishikawa diagram)
- Pareto chart (80/20 Rule)
- Scatter diagram (Shewhart Chart)
- Control chart
- Implementation of 7QC tools End of Training Programme
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