Zephyr Biomedicals - A Division of Tulip Diagnostics (P) Ltd.

Ensure conformity of the manufactured devices are appropriate and checked in accordance with the Quality Management system, before the device is released. Preparation of Technical documentation and the EU declaration of conformity are as per the requirements. Compliance of Post-market surveillance obligations in accordance with the (EU) Regulations. Ensure appropriate practices are followed in accordance with Vigilance & reporting of serious incidents and Field safety corrective actions.