Integrate your management systems to reduce duplication and improve efficiency. If you are currently running separate management systems, get in touch to see how you could make potential savings.

Integrated Management System(IMS) integrates all components of a business into one comprehensible system so as to enable the achievement of its purpose and mission in terms of achieving e.g. Quality (ISO 9001:2015), Environmental (ISO 14001:2015) and occupational health and safety (ISO 45001:2018) objectives. Similarly other management systems components can also be clubbed.

In practice, an integrated management system involves merging existing formal systems and implementing specific best practices organization-wide.

Benefits to the business

Implementation of integrated management systems could result in:

• Avoiding duplication of effort
• Making more effective use of senior management time
• Using resources to implement and manage systems in a more efficient manner
• Achieving more cost efficient certification
• Reducing audit fatigue

A culture and track record of integrated management systems is proof that you are committed to enhancing performance while remaining cost effective, increasing employee and customer satisfaction, and facilitating continuous improvement.

Accreditation Services - ISO 15189 & 17025

ISO 15189 - Medical laboratories - Requirements for quality and competence
ISO Bahrain Consultancy services company objective is to implement ISO 15189 - Medical laboratories - Requirements for quality and competence which meets both the technical competence and the management system requirements that are necessary for it to consistently deliver clinically valid results in line with the requirements & compliance, considering statutory & regulatory, client requirements We assist client in terms of technical and commercial analysis in choosing right certification or accreditation bodies and ensure that certificate or accreditation will be awarded after successful implementation.

ISO 17025 Laboratory Competence
ISO/IEC 17025 is applicable to all laboratories regardless of the number of personnel or the extent of the scope of testing and/or calibration activities. When a laboratory does not undertake one or more of the activities covered by ISO/IEC 17025. ISO/IEC 17025 is for use by laboratories in developing their management system for quality, administrative and technical operations. Laboratory customers, regulatory authorities and accreditation bodies may also use it in confirming or recognizing the competence of laboratories. "

To ensure continual improvements, organization must follow implemented ISO standards to get benefits by performing process audit, monitor, establish and maintain fine tune of records in order to meet quality objectives and customer satisfaction.

We provide an independent, objective service that will continually improve your systems, business performance and customer satisfaction.

We offer a competitive annual maintenance package and audit service to ensure that you continually gain the benefits of ISO certification.

Support Services

• Annual Maintenance Contracts for all the management system standards.
• Total Quality Management (TQM), Six Sigma and GMP.
• CE Markings / GCC, Saudi Standards, Metrology and Quality Organization (SASO)
• Capability Maturity Model Integration (CMMI) – Level 1 to Level 5.
• Bar Coding, Hardware & Application Development Solutions.
• Third party auditing services
• Certification Services
• Industrial Equipment Testing & Inspection
• Automotive Consultancy Services
• SABER Systems

Feasibility Studies

We provide systematic business feasibility studies for various types of manufacturing industry and our core methodology main areas as follows:

• Gap Analysis
• Process Study
• SWOT Analysis
• Reporting

Head Hunting / HR Support

We provide staffing services & assist clients in selecting the right candidates.

This intensive course enables participants to develop the necessary expertise to audit a Quality Management System (QMS) based on ISO 9001:2015 and ensure that the organization is competent in maintaining its quality management systems. The Lead Auditor training will equip participants with the skills and ability to perform audits by applying widely recognized audit principles, procedures and techniques. During this training, the participant will acquire the necessary knowledge and skills to proficiently plan and perform internal and external audits in compliance with ISO 19011; the certification process according to ISO 17021.

Based on practical exercises, the participant will develop the skills (mastering audit techniques) and competencies (managing audit teams and audit program, communicating with customers, conflict resolution, etc.) necessary to efficiently conduct an audit.

QMS Internal Auditor Training

ISO 9001:2015 quality management systems internal auditor training helps develop skills to perform internal audits of quality management systems. This course provides participants with the knowledge and skills to perform internal audits of quality management systems based on ISO 9001, or the equivalent. Participants will learn how to report on the effective implementation and maintenance of a management system in accordance with ISO 19011.

After completing your ISO 9001:2015 internal auditor course, you will understand:

• The concept of the process based quality management system for ISO 9001
• The role of an internal audit in maintaining and improving quality management systems, with reference to the Plan, Do, Check, Act (PDCA) cycle
• The role and responsibilities of an auditor in planning, conducting, reporting and following up on an internal quality management system audit based on ISO 9001, and in accordance with ISO 19011

QMS Awareness Training

The essential objective of QMS awareness training course is to create awareness within the organization regarding various basic requirements of the standard & impart working knowledge on how these requirements can be interpreted to suit the organization’s processes, products, people & customers.

It essentially covers the basic requirements of ISO 9001 & its interpretation & hence helps in providing a great amount of awareness to the group of people in the organization.

Who should attend QMS Awareness Training

• Those who wish to implement quality management system based on ISO 9001 in their organization
• Those who will be required to have the working knowledge essential to motivate the team implementing the quality management system,
• Those who are planning to attend higher level training courses like QMS internal auditor/documentation & implementation/ lead auditor course

Welding Safety Training

"To enhance the employee technical competency in welding safety, mitigating the hazard and risk without affecting welding quality in fabrication division.

In this training course, trainer will guide you through the fundamental of welding safety by explaining step by step process as outlined in the course details. Participants also be taught regulatory & standards requirements and how they can be applied using international best practice methods. Using a step-by-step approach, participants will learn how to ensure quality assurance & control, create the necessary documentation, taking corrective and preventive actions, and monitor the welding skills.

A series of hands-on exercises will help participants to learn effectively while also providing information that can be referenced during your organization’s implementation process."

Environmental Management Systems Training

The aim of the course is to develop international standards and monitor evolving methodologies and best practice in the auditing of Environmental Management Systems (EMS).

The training course is designed to allow participants with the applicable skills and knowledge to evaluate and report on the conformance of an environmental management system and effectively implement an environmental management system. It provides the knowledge to develop, manage, and monitor Environmental Management Systems (EMS) suitable to the needs of their organization focusing on environmental risks, activities, characteristics and impacts.

Occupational Health and Safety Management System

"The primary objective of this course is to instruct OH&S auditors in the principles and practices specific to auditing for conformance with the national and international accepted norms and regulations relating to OH&S requirements. Delegates will be assessed in two different ways, a written examination and a continuous assessment of the attitude and performance of the delegate.

It is recommended that delegates should have some prior knowledge of OH&S management systems standards and auditing. However, this is not mandatory as this course is intended for those who are relatively new to management systems auditing, but who have some occupational health and safety background.

Occupational Health & Safety demonstrate your commitment to maintaining optimum health and safety standards and your organization will stand out in the marketplace.

Food Safety Management Systems Training

The course describes the fundamental purpose of a Food Safety Management System (FSMS) as well as the principles, processes and techniques used for the assessment and management of food safety hazards, including the significance of these for FSMS auditors.

This course will provide a deeper insights on how to implement an effective and robust Food Safety Policy in any organization in the food production, supply and consumption chain.

Interpret the requirements of ISO 22000 in the context of an audit of an organization’s FSMS.

Explain the role of an auditor to plan, conduct, report and follow up of a FSMS audit in accordance with ISO 19011.

CE certification and Authorised Representative (AR) services are related to the requirements for selling products in the European Union (EU):

CE certification

• A declaration that a product meets the EU's legal requirements and is allowed to be sold in the EU. CE stands for Conformité Européenne, which translates to "European Conformity" in English. CE certification is required for many products, including medical devices, electronics, and machinery.

Feasibility Studies

• An EU AR is a legal entity that acts as a liaison between a manufacturer outside the EU and the EU's national authorities. The AR verifies that a product meets the EU's compliance requirements and can bear the CE mark. The AR also takes on some of the manufacturer's responsibilities and can answer questions from authorities.

Six Sigma

• Focuses on reducing process variation and improving quality by using data and statistical analysis to identify and fix errors.

Lean Manufacturing

• Focuses on streamlining processes to maximize customer value by removing unnecessary steps and reducing waste.

CE certification

• Hospital accreditation is a process that evaluates a hospital's performance against established standards and helps them improve continuously. It involves a self-assessment and an external peer assessment.

Feasibility Studies

• Laboratory accreditation is a formal recognition earned by organizations proving they are qualified, competent, and comply with international standards. It involves a third-party assessment that follows international standards. Accreditation is a way to ensure that a laboratory's systems and processes are effective and produce valid results

CE certification

• The College of American Pathologists (CAP) Laboratory Accreditation Program is a globally recognized program that certifies the quality of a laboratory's processes and services. CAP accreditation is considered the gold standard for laboratory quality control.