CID as Manufacturer of Medical Devices has the main responsibility to provide to their customers, patients, doctors, nurses, with the outmost standing product quality.
CID Management defines the quality objectives and mission to ensure product and process compliance with EU Directive 93/42 (and subsequent updating), transition towards the MDR (Medical Device Regulation) 2017/745, ISOs and all applicable requirements. CID Quality Policy is based on the following key points:
- Meet Market and Customer’s needs and ensure a continuous production capability with the same high quality and safety
- Keep the Quality System effective and in compliance with Regulatory Requirements
- Increase the knowledge of employees in accordance with the new standards in order to ensure the compliance towards applicable regulatory requirements
- Focus in qualifying suppliers, based on the risk approach in order to ensure high quality of raw materials in accordance with the standards
- Collaborate with partners, doctors to implement our goals and policies.
- Implementing pro-active monitoring of the products through an effective PMS (Post Market Surveillance) strategy in accordance to Art 120(3) MDR
EN ISO 13485
UNI EN ISO 9001
Gender Equality Certification UNI-PDR 125/2022