|Type of Industry||IT and Consulting|
|Type of Service Provider||Consulting Firm|
Having vast industrial experience and expertise, we have established ourselves as trustworthy service provider of ISO 16949 Consultancy Services. Our rendered services are admired by our clients for their high efficiency, dependability and many other features. A team of our deft professionals render these services in a well-organized manner and within a promising time-frame so as to provide maximum satisfaction to our clients. Moreover, we show lenient behavior to all consumers and fulfill their needs accordingly.
This training has been designed to equip participants with the knowledge and skills needed to assess and report on the conformance and effective implementation of an occupational health and safety management system.
On completion of this training you will be able to:
The training comprises presentations, workshops and role-play exercises.
Participants are not expected to possess knowledge of auditing, quality management system or OHSAS 18001:2007 before attending the course.
Under this category, we offer NABL Certification, ISO 13485:2003 and ISO 17025 : 2005 Certification.
ISO 13485 Certification (NABL) is an international standard, recognized throughout the world for establishing a business management system specific to the medical device industry. Borrowing the structure of ISO 9001:2008, ISO 13485 is applicable to organizations that manufacture private label medical devices, in vitro diagnostic medical devices, and medical components. Created by the International Organization for Standardization, ISO 13485:2003 is based on quality management principles.
Advantages of Laboratories and Medical Certification
The EU introduced the CE marking scheme to make trade easier and cheaper between EU countries. It means that a manufacturer claims that their product conforms to the minimum legal requirements for health and safety as laid down in EU directives.
Often customers will look for CE marking on a product as an indication of conformance to laid down minimum standards, and therefore a minimum level of quality that other products may lack.
If you manufacture or import a product which falls within the scope of one or more of the New Approach Directives and wish to place your product on the market in any of the members states of the European Economic Area (EEA), then you must apply CE marking to your product against the essential requirements of all these applicable directives.
Product Directives contains the "essential requirements" and/or "performance levels" and "Harmonized Standards" to which the products must conform. Harmonized Standards are the technical specifications (European Standards or Harmonization Documents) which are established by several European standards agencies (CEN, CENELEC, etc).