Clariant: Appointment of Regulatory and ISO 13485 Expert
Clariant Masterbatches appoints a global regulatory and ISO 13485 expert to its Medical and Pharmaceutical team. Dr. Gunther Luebke will be responsible for the ISO 13485 quality system and overseeing the specific regulatory requirements across Clariant’s three sector-dedicated ISO 13485 certified global sites in Lewiston (ME) in the USA, in Malmö in Sweden and in Singapore. He will provide an expert resource for both the Clariant team, and medical and pharmaceutical customers in meeting the increasingly strict controls governing end-product ingredients within this sector.
Gunther Luebke comes with extensive experience in polymers / additives as well as Product safety and general regulatory issues. He was previously part of Clariant’s expert team within the Masterbatch Business Unit on REACH.
Clariant’s Medical and Pharmaceutical segment manages the development, production, marketing and technical support for Clariant’s Mevopur color masterbatches and custom performance compounds. These are manufactured exclusively for medical and pharmaceutical applications.
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