"Welcome to EURO CONFORMITY ASSESSMENT (ECA)"......... we are a internationally recognised Certification Body with offices located in India, UAE, and other countries around the world. ECA provide independent third party certification services for Quality, Food Safety, IT Service, Information Security, Environmental, Health & Safety, management systems to national and international standards, including the ISO 9000 series of standards, ISO 14001, HACCP Warranty/ISO 22000, ISO 20000 and ISO 27001 and provide various other certifications through our various international partners like SA 8000, WRAP, BRC, GlobalGap, Tesco NatureÃƒ¢â‚¬Ã¢â€ž¢s Choice and many moreÃƒ¢â‚¬Ã‚¦.
We also provide product certifications (CE Mark) through our various network partners in the various EU directives on Medical Devices, Construction Equipments, Lifts, Cranes, Machinery, LVD and EMC.
We also provide consulting services in the filed of ISO 17025, API, GMP, WHO-GMP etc. We are very customer focused and we offer value-added service, as we believe that auditing should be for continual improvement rather than just a regular check to ensure that requirements are being complied with. We endeavour to give companies the true benefits of certification. We offer services without any discrimination and maintain highest ethical standards.
We provide packages to aid in the implementation of the ISO 9000 and ISO 9001 quality certification requirements and make your business by giving proper Certification of ISO 9001:2008 Certificate,ISO 14001:2004 Certificate,ISO 22000:2005 Certificate,OHSAS 18001:2007 Certificate,ISO 27001: 2005 Certificate,ISO 13485: 2005 certification and also provide the ISO Training.
ISO 9001:2008 is the world's most recognised quality certification standard. The familiar three standards ISO 9001, ISO 9002 and ISO 9003 have all been integrated into the new ISO 9001:2008. The standard specifies requirements for a quality management system for any organisation that needs to demonstrate its ability to supply products/services that consistently meet the customer and regulatory requirements whilst enhancing customer satisfaction.
SO 14001:2004 is the world's most recognised environmental management certification standard. Environmental management system certification, ISO 14001, basically requires the organistion to monitor and manage its impact on the environment. By controlling risks and creating improvements, not only will the organisation be protecting the environment but will also bring bottom line benefits to the performance of the company. There is also the added advantage that the standard requires the company to be aware of all the legislative requirements
The (OHSAS) specification gives clearer direction to an occupational health and safety management system. OHSAS 18001:2007 is an audit/certification specification, not a legislative requirement or a guide to implementation. It should be noted that OHSAS 18001:2007 does not state specific performance criteria, or give detailed specifications for the design of a management system. Instead, the system is geared towards reducing and preventing accidents and accident-related loss of lives, resources, and time. OHSAS 18001:2007 has been developed to be compatible with the ISO 9001 (Quality) and ISO 14001 (Environmental)
Food Safety Management Systems -- Requirements for any organization in the food chain. ISO 22000 is a new International Standard designed to ensure safe supply of foodstuff throughout the entire supply chain on a worldwide basis.
Information is now globally accepted as being a vital asset for most organizations and businesses. As such, the confidentiality, integrity, and availability of vital corporate and customer information may be essential to maintain competitive edge, cash-flow, profitability, legal compliance and commercial image. ISO 27001 is intended to assist with this task. It is easy to imagine the consequences for an organization if its information was lost, destroyed, corrupted, burnt, flooded, sabotaged or misused. In many cases it can (and has) led to the collapse of companies.
ISO 13485 is an international standard that specifies requirements for regulatory purposes for medical device manufacturers. It provides a framework for companies to meet their customer and regulatory requirements. It is becoming widely accepted as the international standard to address medical device requirements around the world. The main goal is to provide a harmonized model for quality management system requirements in the international market since different countries might have different standards. While it remains a stand- alone document
Euro Conformity Assessment
Ms. Payal Goyal
Cabin No. 28, IInd Floor,
S.C.O. 41, Sector-11,
Panchkula Ãƒ¢â‚¬“ Haryana Ãƒ¢â‚¬“ 134 109
Email :- [email protected]
Visit the Author's website: http://www.eca.net.in