M
Mark W
Could somebody clearify for me the main advantages/disadvantages of certifying to QS-9000 as either a corporate scheme or certifying each site independently. In particular, how should I interpret the condition that the quality system must be centrally structured and managed? Does this imply that the Level I and II documents must be identical for each site with a corporate scheme, since I believe there is only one document review for this type of certification? How about a comparison of typical costs for a company with a corporate division and two manufacturing facilities located accross the country from each other.