Each standard has its unique challenges. ExoLytic assists its clients in surmounting these challenges and transforming what may appear to be burdens, into tools which management can leverage to achieve its goals. Exolytic helps companies identify opportunities for continuous improvement by showing them how to measure performance, analyze data, and apply that information to their operations. 

ISO 9001

ISO 9001 sets a standard that focuses on the principles for a quality management system (QMS).  It assists businesses and organizations to succeed by improving efficiency, increasing productivity, and enhancing customer satisfaction. ISO 9001 is fitting for all types of organizations, regardless of its size, or field of service. Implementing ISO 9001 will evaluate the complete framework of your company to define who is affected by your work, what they expect from you, and it will facilitate a clear vision of your objectives and uncover new business opportunities.

AS 9100

AS 9100 is primarily intended for use by the aviation, space, and defense organizations. AS 9100 uses the essentials of ISO 9001 to develop the requirements and proposals to outline the sensitive nature of aerospace industries. The standard system offers suppliers a complete quality system for providing safe and reliable products to the aerospace industry. Implementing AS 9100, a company is establishing a commitment to ensuring constancy in its products, while creating a strong reputation for its dependability.

ISO 17025

ISO 17025 is the main ISO standard used by testing and calibration laboratories.  It specifies the general requirements to carry out tests and calibrations, including sampling. The standard will cover testing and calibration performed using regular methods, non-regular methods, and laboratory developed methods.  ISO 17025 is applicable to all organizations performing tests and calibrations. These include, for example, first-, second- and third-party laboratories, and laboratories where testing and calibration forms part of inspection and product certification. To be deemed competent, most labs must hold accreditation to the  ISO 17025 standard.  In most cases, suppliers and regulatory authorities will not accept test or calibration results from a lab that is not accredited.

ISO 27001

ISO 27001 is a system that helps to manage, monitor, audit, and improve an organization’s information security.  It helps manage all security matters in one place with a consistent and cost-effective system. Using this standard will assist an organization on how to manage the security of assets, such as financial information, intellectual property, employee details or information entrusted to you by third parties.  ISO 27001 is an efficient approach to managing sensitive company information and will ensure that risk mitigation is implemented to remain secure. This standard will benefit all small, medium, or large businesses in any area that wishes to keep information assets secure.

ISO 14001

ISO 14001 offers useful tools for all kinds of companies and organizations looking to manage their environmental responsibilities. It maps out a framework that can be followed to set up an effective system, which can be used to improve environmental performances while maximizing the use of resources and gaining a competitive advantage, but also reducing waste.  ISO 14001 focuses on specific approaches such as audits, communications, setting objectives, and product life cycle analysis, as well as environmental challenges, such as climate change. It gives a company or organization the ability to demonstrate compliance with current and future legal requirements.

ISO 13485

Safety and quality are two of the most important factors when it refers to the medical device industry.  ISO 13485 lays out the requirements for a quality management system, where a company or organization must demonstrate its ability to provide medical devices and related services that regularly meet customer and regulatory requirements.  ISO 13485 is designed to be used by organizations involved in the design, production, installation, and servicing of medical devices or related services. By implementing ISO 13485, a company or organization will assert a commitment to the safety and quality of medical devices, while also providing a practical basis for manufactures to address the medical devices regulations and responsibilities.

ISO 45001

ISO 45001 helps organizations reduce the burden of work-related injuries and diseases by providing a plan to improve employee safety, reduce workplace risks, and create better and safer working conditions. The matter of work-related injuries and diseases are important, both for employers and the wider economy. By implementing ISO 45001, companies can reduce losses from early retirements, staff absence, and rising insurance premiums. This system gives guidance on how to manage it and enables organizations to provide safe and healthy working conditions by preventing injuries and considering any potential for disaster.  ISO 45001 is applicable to any organization wishing to improve their health hand safety requirements, while eliminating hazards and minimizing risks.


Other services being offered:

  • Knowledge Management
  • Integrated Management Systems
  • Internal Auditing
  • Supplier Audits
  • Sub-contractor Audits
  • Lean Manufacturing
  • Six Sigma
  • Root Cause and Risk Analysis
  • Restriction of Hazardous Substance (RoHS)
  • Supply Chain Management
  • Quality Support
  • and more