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  • ISO 13485
  • CE Marking
  • cGMP
  • Inspections & Auditing
  • LEAN (TPS)
  • BSCI
  • SA8000
  • ISO 45001 - OHS
  • ISO 27001 - ISMS
  • ISO 9001 - QMS
  • ISO 14001 - EMS
ISO 13485 CE Marking cGMP Inspections & Auditing LEAN (TPS) BSCI SA8000 ISO 45001 - OHS ISO 27001 - ISMS ISO 9001 - QMS ISO 14001 - EMS

who we are

Business Management Consultants International is the Leading Business Management Consulting Organization for Management System, Social Compliance and All Buyers Code Conduct Consultancy, Training, Documentation and Facilitation Services Provider.
Business Management Consultants International has been in the field of Consultancy since 2006 and has thus acquired an extensive expertise in the field Management System Consultancy & Training Services.
Our keen knowledge in the field of Consultancy has helped us to develop Management System that answers the needs of today’s clients.

These Management Systems allow you to:

  • Increase productivity
  • Reduce operating costs
  • Increase customer satisfaction

why choose us

  • WE ARE PASSIONATE
  • HONEST & DEPENDABLE
  • ALWAYS IMPROVING

CE Marking

CE Marking  The CE marking is the manufacturer's declaration that the product meets the requirements of the applicable EC directives. It is often taken to be an abbreviation of Conformité Européenne, meaning "European Conformity". The CE marking indicates a product’s compliance with EU legislation and so enables the free movement of products within the European market. By affixing the CE marking to a product, a manufacturer declares, on his sole responsibility, that the product meets all the legal requirements for the CE marking, which means that the product can be sold throughout the European Economic Area (EEA, the 28 Member States of the EU and European Free Trade Association (EFTA) countries Iceland, Norway, Liechtenstein). This also applies to products made in
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ISO 13485

ISO 13485, Medical devices – Quality Management Systems – requirements for regulatory purposes, is an internationally recognized standard for organizations involved in the medical device industry.  Companies are using compliance to this standard to obtain the certification of their Quality Management System. The primary purpose of the ISO 13485 standard is the Harmonization of the Medical Device regulatory requirements for Quality Management Systems. Whether you are looking to operate internationally or expand locally, ISO 13485 Certification can help you improve overall performance, eliminate uncertainty, and widen market opportunities. Companies with this certification communicate a commitment to quality to both customers and regulators.
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ISO 27001:2013

ISO 27001 (formally known as ISO/IEC 27001:2005) is a specification for an information security management system (ISMS). An ISMS is a framework of policies and procedures that includes all legal, physical and technical controls involved in an organisation's information risk management processes. Certification to ISO 27001 allows you to prove to your clients and other stakeholders that you are managing the security of your information.  According to its documentation, ISO 27001 was developed to "provide a model for establishing, implementing, operating, monitoring, reviewing, maintaining and improving an information security management system.ISO/IEC 27001 specifies a management system that is intended to bring information security under management control and gives specific requiremen
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Software Validation

In software project management, software testing, and software engineering, verification and validation is the process of checking that a software system meets specifications and that it fulfills its intended purpose. It may also be referred to as software quality control. Software Validation is a process of evaluating software product, so as to ensure that the software meets the pre-defined and specified business requirements as well as the end users/customers' demands and expectations. We perform software validation as per the requirements of ISO 13485 Clause 4.1.6. Validation of software is conducted in the company premises under operation's environment. Software is tested/validated and validation report is provided to the customer.
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