Product life cycles are managed in the manner specified in Innokas Medical’s quality system so that they meet the official regulations and standards set for medical and in vitro devices.
Everything stems from a satisfied end customer, which may be a doctor, a hospital staff member, or a hospital maintenance person. As the age of a product increases, it becomes necessary to carry out maintenance procedures. In some cases these procedures involve processing a customer complaint, which may lead to a product revision or even an on-site technical update of the product. Innokas Medical can do all of this for our customers in a manner specified in our quality system and approved by officials.
As the age of a product increases, the need for maintenance procedures grows, and in some cases it is necessary to carry out updates due to changes in the environment. If ROHS or other similar needs so dictate, our maintenance planning and documentation offer product revisions and product documentation updates. Product data are managed within Innokas Medical’s systems, or if a customer so desires, they are updated directly within the customer’s product data management system.
Life cycle management philosophy is a very important part of producing health technology and manufacturing healthcare devices. We at Innokas Medical understand this — we have done it already since 1994.