VR Global Consulting

(An ISO 9001:2015 Certified Company)

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Discover > Document > Improve

Sometimes the messiest processes need an outside perspective. We work on-site with your team to quickly discover, document and improve your processes, helping you remove bottlenecks, reduce errors, and resolve confusion and conflicts among your staff. Our methodology has been refined over a combined 20+ years working both as an in-house and an independent consultant. You get results, and we get them fast.


Process Discovery

Discovery - The first step in getting control of your processes.

Why start with process discovery? Why not just jump straight into process improvement? If we don't all agree on where we are now, it's nearly impossible to plan a route to where we want to go.

So, the first job is to get the process out of people’s heads and into the daylight where we can all work on it as a team.

The classic way to way to do this is to build a map of the steps with the people who use it. And it's still the best way. Getting process down in black and white, or at least on a whiteboard, reduces the chance of people talking about the same process but having a different understanding of it.

We do that by leading small groups of the actual process users through the steps on a whiteboard, a screen or a wall. Very often few people have seen the whole process, and there are always some surprises.


Process Documentation

Documentation - Creating a process library

A whiteboard is a great tool for exposing the process but not much good for recording and communicating it to the rest of the organization. You need a means of publishing your processes in a single, easily accessible, editable place.

Imagine being able to view every one of your processes in a single online hub, with both staff and new hires able to view their individual roles and click on any individual task to pull up all associated documents and instructions. We help in all such activities.

Fast Track Process Improvement


Process Improvement

Once we have captured the existing process, we can shift to process improvement projects. For this, we use a simplified mix of Lean and Six Sigma methodologies called Fast Track Process Improvement.

This is tailored for the complexity of back-office processes. No off-putting jargon or "analysis paralysis", just straight forward improvement projects with properly allocated responsibilities and accountability.

You and your staff already know all the important stuff: the exceptions, the confusion over roles, the bottlenecks, the problem areas, the inefficiencies... everything. Our job is to get all the pain points and bottlenecks listed and prioritized.

Surprisingly, at least to some executives and business owners, many of the ideas come from the users themselves. Ideas that have been latent in their organizations for a while. We give people the opportunity to express them.



  • ISO 9001 (Quality Management Systems)

specifies requirements for a quality management system when an organization:

a) Needs to demonstrate its ability to consistently provide products and services that meet customer and applicable statutory and regulatory requirements, and

b) Aims to enhance customer satisfaction through the effective application of the system, including processes for improvement of the system and the assurance of conformity to customer and applicable statutory and regulatory requirements.

All the requirements of ISO 9001 are generic and are intended to be applicable to any organization, regardless of its type or size, or the products and services it provides.




  • ISO 14001 (Environment Management System)

An environmental management system helps organizations identify, manage, monitor and control their environmental issues in a “holistic” manner. It requires that an organization considers all environmental issues relevant to its operations and resources’ use and efficiency.
This includes the need for continual improvement of an organization’s systems and approach to environmental concerns.




  • ISO 45001 (Occupational Health & Safety Management System)

The occupational health and safety (OH&S) management system, is a new international standard that provides a framework for an organization to manage risks and opportunities to help prevent work-related injury and ill health to workers. The intended outcome is to improve and provide a safe and healthy workplace. All of its requirements are designed to be integrated into an organization’s management and business processes.




  • ISO 22000 (Food Safety Management System)

Sets out the requirements for a food safety management system (FSMS) and can be certified to. It maps out what an organization needs to do to demonstrate its ability to control food safety hazards in order to ensure that food is safe.



  • Fassai (Food Safety and Standards Authority of India)

We do the Basic, State and Central certification for Fassai. A food license by which is issued by the FSSAI is regarded as a permit which is required to operate a food-related business and also in order to ensure good quality of food in your business and for the benefits one from government actions on non-compliances.




  • ISO 20000 (Information Technology Service Management)

ISO 20000 is the international IT service management (ITSM) standard that enables IT organizations in-house, outsourced or external to ensure that their ITSM processes are aligned both with the needs of the business and with international best practice. Helps organizations benchmark how they deliver managed services, measure service levels and assess their performance.




  • ISO 27001 (Information Security Management System)

Is the international standard that describes the requirements for ISMS (information security management system). ISO 27001 is supported by its code of practice for information security management, ISO/IEC 27002:2013. Achieving accredited certification to ISO 27001 provides an independent, expert assessment that information security is managed in line with international best practice and business objectives.




  • ISO 13485 (Standard for Medical Devices)

Specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. This can also be used by suppliers or external parties that provide product, including quality management system-related services to such organizations.



  • CE Marking

CE marking is a mandatory conformity marking for certain products sold within the European Economic Area (EEA) since 1985.[1]The CE marking is also found on products sold outside the EEA that are manufactured in, or designed to be sold in, the EEA. This makes the CE marking recognizable worldwide even to people who are not familiar with the European Economic Area. It is in that sense similar to the FCC Declaration of Conformity used on certain electronic devices sold in the United States.
The CE marking is the manufacturer's declaration that the product meets the requirements of the applicable EC directives.



  • GMP (Good Manufacturing Practice)

A GMP is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.




  • GDP (Good Distribution Practice)

Good distribution practices ensure maintaining product safety and quality during distribution across the supply chain and this practice is of significant importance for the pharmaceutical industry. Good Distribution Practices (GDP) Compliance report for Pharmaceutical Industry demonstrates Quality commitment & sound practices in the entire pharmaceutical distribution supply chain.



  • MSME:

We help in getting the MSME certification to your organization.



  • 5S

5S Certification, Implementation and Training




  • ISO/IEC 17021-1:2015

Conformity assessment — Requirements for bodies providing audit and certification of management systems — Part 1: Requirements ISO/IEC 17021-1:2015 contains principles and requirements for the competence, consistency and impartiality of bodies providing audit and certification of all types of management systems. Certification bodies operating to ISO/IEC 17021-1:2015 do not need to offer all types of management system certification. Certification of management systems is a third-party conformity assessment activity and bodies performing this activity are therefore third-party conformity assessment bodies.



  • ISO 21001:2018

Educational organizations — Management systems for educational organizations — Requirements with guidance for use ISO 21001:2018 specifies requirements for a management system for educational organizations (EOMS) when such an organization: a) needs to demonstrate its ability to support the acquisition and development of competence through teaching, learning or research; b) aims to enhance satisfaction of learners, other beneficiaries and staff through the effective application of its EOMS, including processes for improvement of the system and assurance of conformity to the requirements of learners and other beneficiaries. All requirements of ISO 21001:2018 are generic and intended to be applicable to any organization that uses a curriculum to support the development of competence through teaching, learning or research, regardless of the type, size or method of delivery. ISO 21001:2018 can be applied to educational organizations within larger organizations whose core business is not education, such as professional training departments.

ISO 21001:2018 does not apply to organizations that only produce or manufacture educational products.



  • ISO/IEC 17025 testing and calibration laboratories

ISO/IEC 17025 enables laboratories to demonstrate that they operate competently and generate valid results, thereby promoting confidence in their work both nationally and around the world. It also helps facilitate cooperation between laboratories and other bodies by generating wider acceptance of results between countries. Test reports and certificates can be accepted from one country to another without the need for further testing, which, in turn, improves international trade.



  • ISO 37001 Anti-bribery management systems

Prevent, detect and address bribery by adopting an anti-bribery policy, appointing a person to oversee anti-bribery compliance, training, risk assessments and due diligence on projects and business associates, implementing financial and commercial controls, and instituting reporting and investigation procedures.



  • ISO 4427:2019

ISO 4427-1:2007Plastics piping systems — Polyethylene (PE) pipes and fittings for water supply — Part 1: General ISO 4427-2:2019Plastics piping systems for water supply, and for drainage and sewerage under pressure — Polyethylene (PE) — Part 2: Pipes ISO 4427-3:2019Plastics piping systems for water supply, and for drainage and sewerage under pressure — Polyethylene (PE) — Part 3: Fittings


  • NABH Accreditation

Want to earn recognition for your hospital? Get the NABH accreditation!

Getting NABH Accreditation for a hospital is both prestigious as well as mandatory. It boosts patient confidence in the hospital and is a great tool for promoting medical tourism and boosting revenue and goodwill for the hospital.

While the process of getting the accreditation is complex and cumbersome, our professional NABH consultants will make the task seamless for you!

We will walk you through the complex procedure with 600+ objective elements and assist you through each and every process of both patient centered standards and organization centered standards. Our NABH consultants will assist with systems, procedures and software to ensure that transparency is maintained and protocols are stringently followed to avail the NABH Accreditation. If you are planning to construct a new hospital building, we will design it for you in accordance with the NABH standards for hospital buildings! For existing buildings, we will suggest changes to upgrade your hospital for NABH!


  • NABL Accreditation

Get more clients and business with internationally recognized NABL Accredition!

We offer NABL certification consultancy services to assist you at every step of getting the NABL accreditation. Right from filling up the application form for the accreditation to following quality checks and control and documentation, we will do it all for you. Our NABL consultants will

  1. Carry out an internal audit of your system
  2. Assist you in preparation of Standard Operating Procedures for each test being carried out in your lab
  3. Ensure with the calibration of equipment and lab instruments
  4. Ensure that all the environment parameters related to temperature, storage placement, humidity etc are maintained
  5. Prepare all the essential documentation required to be submitted to the NABL accreditation authority
  6. Since we do all the hard work for you, your lab is assured of being NABL certification at the soonest!
  • JCI Accreditation

Get the Gold Seal of Approval for your medical facilities and win the trust of patients across the globe!

JCI Accreditation is the ultimate certificate of providing world class healthcare.Once a medical facility is JCI Accredited, it automatically earns the respect of the international medical tourists. As such, if you want your hospital to be found on the world map, JCI Accreditation is the way to go!

JCI has laid down stringent quality norms encompassing more than one thousand measurable elements. Our JCI consulting team members will assist you at every step, every process so that your facility gets the JCI accreditation at the soonest.

  1. Our JCI consulting team will assist you with:
  2. Documentation and timely submission of the same to the JCI
  3. Prepare report with accurate information through all the phases of accreditation process
  4. Gear the hospital site, processes and procedures in line with the JCI norms to make it “survey ready”
  5. Initiating quality improvement system and ensuring implementation of the same
  6. Ensuring patient safety and patient care in accordance with the JCI norms
  7. Ensure that the hospital complies with all the standards related to international patient safety goals

It takes at least 2 years to implement all the standards as laid down by the JCI. With our professional JCI consulting team, the experience is going to be hassle free!


  • Online Certificate verification

We do help universities, corporates, recruitment agencies, students make a pool of qualified, talented and confirmed experts, customized to the necessities of industry. Companies today are looking for the best and are recruiting only the ‘cream of the crop’. By adopting to VRGC services, colleges can now ensure their students are not only qualified and skilled, but also verified and are job-ready. It is imperative for any organization to hire genuine candidates with valid education and authentic degrees. At VR Global Consulting, we follow a stringent process when it comes to the verification of certificates provided by candidates. More than mere background checks over the phone, we do a closer analysis of the original copy of certificates provided by a client. We conduct a through review to check the genuineness of the certificates.


Degree Certificate Verification

  1. Name of college and university
  2. Physical mailing address of college
  3. Registration number / Roll number
  4. Issuing date of certificates
  5. Year of Enrollment
  6. Year of passing
  7. Provisional Degree certificates




Foundation Training/Internal Auditor Training/Lead Auditor Training

Foundation training is designed to provide a basic understanding of Quality Management System (QMS)



The ISO internal auditor / lead auditor course gives organizations an opportunity to increase value to their activities and also those who would to like to establish their career as a lead auditor for ISO 9001 and for managers and business owners who would like to implement the Quality Management System in your organizations


Internal Auditor Training: ISO Internal Auditor course is a professional course that  is generally a one or two days Course depending on the standard requirements. ISO internal auditor courses enables you to utilize your recently procured abilities to overview any process related conditions in your organization. Compose the review report and make restorative move, and examining contextual investigations to create abilities for recognizing and managing the nonconformance.


Lead Auditor Training: 5 days, lecture type or online training carried out through an experienced registered ISO lead auditor as facult(y)ies.



  • You will gain Internationally valid Lead auditor certificate .
  • Qualifies the individual for third party auditing.
  • Qualified Individuals helps the organization to train and provide guidance for implementation of Management systems.
  • Qualified Lead Auditor can train and provide certificate to Internal Auditors.
  • Provides professional assistance to the Top Management in continually improving the organization’s Management System towards organizational goal.


Currently our Foundation Training programmes are offered for the following ISO standards:

  • ISO 9001:2015
  • ISO 27001:2013
  • ISO 22000:2018
  • ISO 14001:2015
  • OH&S 45001:2018

ELIGIBILITY:- Understand English language (as the seminar will be in English)


SCHEDULE:- As per calendar.


FEES: - As per calendar. Time: - As per calendar.



Any individual, Business owners, fresh or experienced employees, College outgoing final year students, Job aspirants can participate in the course. Prior exposure or experience in the Management System environment will be an added advantage but not necessary.