Iso 13485 Certification
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CDG Inspection Ltd.ISO 13485:2003 specifies requirements for a quality management system where an organization needs to demonstrate its ability to pro...View Product Details
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Key Features
CDG Inspection Ltd.ISO 13485:2003 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer requirements and regulatory requirements applicable to medical devices and related services. The primary objective of ISO 13485:2003 is to facilitate harmonized medical device regulatory requirements for quality management systems.
Design and develop medical devices to international quality standards, ensure smooth submission, meet ISO 13485 standards, satisfy customers and keep ahead of all regulatory developments with our medical devices training courses.
ISO 13485 is an ISO Standard, published in 2003, that represents the requirements for a comprehensive management system for the design and manufacture of medical devices. It's the quality management standard specifically designed for organizations that provide medical devices or related services to ensure that customer and regulatory requirements are consistently met
ISO 13485 is the quality standard designed for medical device manufacturers. ISO 13485 is also an international standard that is commonly used as the basis of regulatory compliance for the FDA. If you are a medical device manufacturer, BioMed/Pharma, or perform work with medical device manufacturing or distribution, ISO 13485 is an essential quality standard for your organization.
Design and develop medical devices to international quality standards, ensure smooth submission, meet ISO 13485 standards, satisfy customers and keep ahead of all regulatory developments with our medical devices training courses.
ISO 13485 is an ISO Standard, published in 2003, that represents the requirements for a comprehensive management system for the design and manufacture of medical devices. It's the quality management standard specifically designed for organizations that provide medical devices or related services to ensure that customer and regulatory requirements are consistently met
ISO 13485 is the quality standard designed for medical device manufacturers. ISO 13485 is also an international standard that is commonly used as the basis of regulatory compliance for the FDA. If you are a medical device manufacturer, BioMed/Pharma, or perform work with medical device manufacturing or distribution, ISO 13485 is an essential quality standard for your organization.
Explore in hindi - आईएसओ 13485 प्रमाणन
Company Details
CDG INSPECTION LTD., Established in 2001 at Mumbai in Maharashtra, is a leading service provider of ISO Certification Consultants in India. CDG INSPECTION LTD. is one of Trade India's verified and trusted names for listed services. With extensive experience in the field of ISO Certification Consultants, CDG INSPECTION LTD. has made a reputed name for itself in the market with satisfactory Authentic Kosher Certification Services, BIFMA Certification, Best Ce Marking Certification In Mumbai, etc.
Focusing on a customer-centric approach, CDG INSPECTION LTD. has a pan-India presence and caters to a huge consumer base throughout the country. Get ISO Certification Consultants from CDG INSPECTION LTD. at Trade India quality-assured services.
Focusing on a customer-centric approach, CDG INSPECTION LTD. has a pan-India presence and caters to a huge consumer base throughout the country. Get ISO Certification Consultants from CDG INSPECTION LTD. at Trade India quality-assured services.
Business Type
Service Provider
Employee Count
25
Establishment
2001
Seller Details
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CDG INSPECTION LTD.
Marketing Manager
Ms Nishi
AddressView on Map
G-3, Gokuldham, Goregaon East, Mumbai, Maharashtra, 400063, India
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