K S CONSULTANTS
Iso in North West Delhi
iso-cemarking-consultancy.com/
Address
1370 B Jain Nagar Delhi. Rohini Sector 5.. P.C. 110085, North West Delhi, North West Delhi.What you should know about K S CONSULTANTS
Get following certification at very economical cost:
ISO 9001:2008/ISO 9001:2015(Latest)
ISO 14001
ISO 18001
ISO 20000
ISO 22001
ISO 27001
ISO 13485
HACCP
CMMI
IEC
GMP
CE Marking
Rohs Certification
Bifma Certification
For Further Details contact under signed
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Deepak - 09310585525/09811238993
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- The services are provided by our team members (Engineer and M.B.A). having rich experience of many companies.
- Our training kit is a good tool to establish and implement ISO and establish better control in routine work, reduce cost and improve profitability.
- In ISO area consultancy, we are having leading name in Market and having branded image of 100% success rate.
- Timely completion of work and provide highest customer satisfaction. Payback of our consultancy cost is 2 months.
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ISO 9001 :2015ISO 9001:2015 specifies requirements for a quality management system for any organization.
ISO 14001: 2015 specifies requirements for a environment management system for any organization.
OHSAS is the Occupational Health and Safety Assessment Series for health and safety management systems.
The definition and aim of the RoHS directive is quite simple. The RoHS directive aims to restrict certain
ISO/IEC 17025 was first issued in 1999 by the International Organization for Standardization (ISO)
SO/TS 16949 was jointly developed by The International Automotive Task Force (IATF) members
ISO 22001 /HACCPInternational Organization for Standardization (ISO) has published ISO 22001:2015 - Food Safety Management .
ISO 27001 :2015The goal of ISO 27001:2015 is to provide a common base for developing organizational information security policies.
ISO 13485: 2015 is an international standard that represents the needs for a comprehensive quality management system for the design and manufacture of medical devices. Though it is tailored to the industry's quality system expectations and regulatory necessities, an organization does not require being actively manufacturing medical devices or their components to look for certification to this standard.
CE marking is an European conformity mark. CE marking on a product indicates that the product complies with legal requirement of European market. and the same can be sold with in European Union. CE Marking ensures that a product meets a minimum safety standard and product does not compromise with public safety. CE Marking is also applicable for manufacturers located outside European Union if they want to place their product in European union. CE Marking requirements are mentioned in different EU directives
A GMP is a system for making sure that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.GMP is an abbreviation for Good Manufacturing Practices.
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