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ISO 45001

What is ISO 45001 ISO 45001 is an International Standard that specifies requirements for an occupational health and safety (OH&S) management system, with guidance for its use, to enable an organisation to proactively improve its OH&S performance in preventing injury and ill-health. ISO 45001 is intended to be applicable to any organisation regardless of its size, type and nature. ISO 45001 enables an organisation, through its OH&S management system, to integrate other aspects of health and safety, such as worker wellness/wellbeing; however, it should be noted that an organisation can be required by applicable legal requirements to also address such issues: • Improving its ability to respond to regulatory compliance issues • Reducing the overall costs of incidents • Reducing downtime and the costs of disruption to operations • Reducing the cost of insurance premiums • Reducing absenteeism and employee turnover rates • Recognition for having achieved an international benchmark (which may in turn influence customers who are concerned about their social responsibilities) .

ISO 45001 Model:


Any organization can benefit from implementing ISO 45001 as its requirements are underpinned by eight universal management principles.

  • Customer focused organization.
  • Leadership.
  • Involvement of people.
  • Ensuring process approach.
  • Systematic approach to management.
  • Factual approach to decision making.
  • Mutually beneficial supplier relations.
  • Continuous improvement.

ISO 45001

ISO 45001 Its primary objective is to facilitate harmonized medical device regulatory requirements. The standard contains specific requirements for manufacture, installation and servicing and calls for:

Implementation of a Quality Management System with several enhancements Risk Management approach to product development and product realisation Validation of processes Compliance with statutory and regulatory requirements Effective product traceability and recall systems

Approach and Methodology

ISO 45001 Certification:

  • Gap Analysis.
  • Initial Aspect Identification and Impact Assessment.
  • stablishing the Control.
  • Establishing the documentation.
  • Implementation.
  • Internal Audit.
  • Management Review.
  • Stage I Audit.
  • Stage II Audit.

Clients Testimonials

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Sharaf DG

An excellent well-balanced team with realism about the critical factors determining an invention's viability. Skillful and well-received engagement with the ISO team.


Kayzed is an outstanding business management consultant. I was very pleased with their knowledge and in-depth understanding of what it takes for a ISO Certification. The management's knowledge, natural instincts for business, and ability to put complex transnational business concepts into succinct and easy to understand terms were a great service to me and my team.