ISO 45001 Certification

ISO 45001, one of the world's much anticipated standards for occupational health and safety (OHS), has been approved as a Draft International Standard..
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Every 15 seconds, a worker dies from a work-related accident or disease, and 153 people experience a work-related injury. These represent an enormous burden for organizations and society as a whole, costing over 2.3 million deaths a year, not to mention the more than 300 million non-fatal accidents*.

Now, with ISO 45001 at the Draft International Standard (DIS) stage, the world is one step closer to a robust and effective set of processes for improving work safety in global supply chains. Designed to help organizations of all sizes and industries, the future standard is expected to reduce workplace injuries and illnesses around the world.
More than 70 countries are directly involved in the creation of this important document, being developed by project committee ISO/PC 283, Occupational health and safety management systems, with the British Standards Institution (BSI) serving as the committee secretariat.
“Implementing a strong occupational health and safety management system helps organizations reduce accidents and ill health, avoid costly prosecutions, perhaps even reduce insurance costs, as well as create a culture of positivity in the organization when its people see that their needs are being taken into account,” explains David Smith, Chair of the committee. “Wide adoption of ISO 45001 should reduce the horror stories in the media of poor OHS management leading to loss of life, injury and large-scale disasters, as seen in the factory buildings around the world.”
ISO 45001 is based on the common elements found in all of ISO’s management system standards, assuring a high level of compatibility with the new versions of ISO 9001, Quality management systems, and ISO 14001, Environmental management systems. It uses a simple Plan-Do-Check-Act (PDCA) model, which provides a framework for organizations to plan what they need to put in place in order to minimize the risk of harm. The measures should address concerns that can lead to long-term health issues and absence from work, as well as those that give rise to accidents.
Now that ISO 45001 has advanced to the DIS stage, national member bodies of ISO have been invited to vote and comment on the text of the standard during the three-month balloting period. If the outcome is positive, the modified document may then be circulated to ISO members as a Final Draft International Standard (FDIS). In the event of an affirmative vote, ISO 45001 is expected to be published as an International Standard by late 2016 / early 2017.

For more details about ISO 45001 certification or if you want your organization certified with ISO 45001, please visit the website : www.best-isocertification.com

ISO 13485:2016 Medical devices -- Quality management systems

ISO 13485 Medical gadgets - Quality administration frameworks - Requirements for administrative reasons for existing is an International Organization for Standardization (ISO) standard distributed without precedent for 1996; it speaks to the necessities for a far reaching quality management framework for the structure and assembling of therapeutic gadgets. This standard overrides prior records, for example, EN 46001 and EN 46002 (both 1997), the recently distributed ISO 13485 (1996 and 2003), and ISO 13488 (additionally 1996). The current ISO 13485 release was distributed on 1 March 2016.

ISO 13485:2016 determines necessities for a quality administration framework where an association needs to exhibit its capacity to give medicinal gadgets and related administrations that reliably meet client and appropriate administrative prerequisites. Such associations can be engaged with at least one phases of the life-cycle, including structure and improvement, creation, stockpiling and appropriation, establishment, or adjusting of a restorative gadget and plan and advancement or arrangement of related exercises. ISO 13485:2016 can likewise be utilized by providers or outside gatherings that give item, including quality administration framework related administrations to such associations.

The essential goal of ISO 13485 was to encourage blended restorative gadget administrative prerequisites for quality administration frameworks. ISO 13485 is a standalone standard. It is generally focused around the structure of ISO 9001, however incorporates some specific prerequisites for medicinal gadgets, for example, hazard dissection, sterile assembling and trace ability.

Necessities of ISO 13485:2016 are material to associations paying little heed to their size and paying little mind to their sort aside from where expressly expressed. Wherever necessities are determined as applying to restorative gadgets, the prerequisites apply similarly to related administrations as provided by the association.

For more details about ISO 13485 certification or if you want your organization certified with ISO 13485, please visit the website : www.best-isocertification.com

ISO/IEC 20000-1:2018

Information Technology Service Management (ITSM)

ISO/IEC 20000 is the primary global standard for IT administration the executives. It was created in 2005 by ISO/IEC JTC1/SC7 and amended in 2011 and 2018. It was initially founded on the earlier BS 15000 that was created by BSI Group.

ISO/IEC 20000 is a worldwide IT standard that licenses associations to display significance and show best practice in IT organization. The standard ensures associations can achieve confirmation based benchmarks to interminably improve their movement of IT organizations. The choice of ISO/IEC 20000 has grown rapidly in the widespread open air theater of IT organization providers and it has transformed into an engaged differentiator for transport of IT organizations. ISO/IEC 20000 is changed in accordance with and comparing to the technique approach described inside ITIL from the Office of Government Commerce (OGC).

The 2018 standard (ISO/IEC 20000-1:2018) includes ten segments, following the abnormal state structure from Annex SL of the Consolidated ISO/IEC Directives, Part 1:

1. Scope
2. Normative references
3. Terms and definitions
4. Context of the organization
5. Leadership
6. Planning
7. Support of the Service Management System
8. Operation of the Service Management System
9. Performance Evaluation
10. Improvement

ITSM Benefits:

• Gives certification to invested individual and customers for the administration of IT administrations.
• Gives a procedure to Information Technology Governance
• Gives the association a world-class stage to execute IT benefits.
• Aides adjust and coordinate the IT Services with the general business system.
• Expand in general authoritative productivity and operational execution
• Market separation because of positive impact on organization renown
• Increments merchant status of your association
• Minimizes inward and outer dangers to administration progression
• Brings your association to consistence with legitimate, administrative, and statutory prerequisites - accomplish ISO 20000 affirmation agreeability.

For more details about ISO 20000 certification or if you want your organization certified with ISO 20000, please visit the website : www.best-isocertification.com