Claes-Göran has been responsible for PLM & business processes at Mölnlycke Health Care (MHC) for decades. He has been instrumental in the definition and rollout of Enovia as a PLM tool in a medical device company which of course is highly regulated.
From document to object orientation - for regulatory requirements
Claes-Göran will tell us about the the road towards PLM at MHC. The medical device industry is highly regulated and PLM is a crucial component in having track of products, processes and information in order to fulfil regulatory requirements. In this presentation Claes-Göran will focus on their way of moving from large complex documents for manual reporting purposes to being more object oriented and automation of the reports. He will also look at how that same information can be re-used in other tools and processes, e.g. product catalogues. This will be an input to a general discussion about the applicability in other industries and perhaps your company in particular.
About Mölnlycke Health Care:
Mölnlycke Health Care is a Swedish medical device company headquartered in Gothenburg and active internationally. The company manufactures and sells wound care and single-use surgical products and is a service provider to the healthcare sector.