Quality assurance
Product quality has its core in the R&D department of a company. With its experienced scientists and engineers ADANI covers the entire R&D spectrum, from the development of products and components through to the integration into complete system solutions. ADANI is committed to providing innovative high quality products and services that consistently meet and exceed the expectations of our customers.
Since 2002 ADANI has been registered by SGS United Kingdom Ltd a Notified Body. to the following ISO Standards — ISO 9001:2000 and ISO 13485, which are recognized and accepted worldwide.
ISO:13485 is an ISO Standard specifically written for Medical Device Manufacturers.
This standard includes the design, development and manufacturer of medical devices for compliance with the CE marking Medical Devices Directive 93/42/EEC Annex II (excluding Section 4) requirements.
Along with the ISO 9001 and ISO13485 registrations, ADANI also holds CE0120 (Certificate No.C56836). CE and CE0120 marking are often referred to as a ’passport’ that allows manufacturers from anywhere in the world to sell their goods throughout the European market. The letters ’CE’ are an abbreviation for Conformité Européenne, French for European Conformity. The letters ’CE’ on a product are the manufacturer’s conformation that the product meets the requirements of all relevant European Directives.
CE marking on a product also indicates:
- to governments that the product can be legally sold within the European Union,
- to customers that the product meets designated credibility, safety standards and therefore have an acceptable level of quality.