Kath Clarke joins Medvance team as Regulatory Affairs Manager
April 07 2010
Medvance are delighted to announce that Kath Clarke has joined the ever expanding Medvance team based in Burn, near Selby in the UK.
Kath brings her many years of expertise in Regulatory Affairs, specifically with Medical Devices and the CE marking process to Medvance, where she will be heading up the Regulatory Affairs Department. Kath's extensive knowledge of the Medical Device Directive and it's practical application will be of huge benefit to those clients needing assistance navigating the complex requirements to get their product CE marked and subsequently to ensure conformity with the appropriate Medical Device Directive, throughout a product's life cycle. Advice can also be provided regarding a company's Quality Management System to ensure that all regulatory requirements are appropriately captured and documented.
If you need any assistance with any aspect of medical device regulatory affairs then please do not hesitate to contact the Medvance offices.