The essential element of our Company’s mission is to safely and efficiently provide the necessary investigational products, auxiliary drugs, and medical devices to patients participating in clinical trials.
To achieve this, we have developed and maintain a quality management system that continuously complies with the guidelines of good pharmaceutical (GMP), distribution (GDP), and clinical practice (GCP) and the requirements of the ISO 9001: 2015 standard.
Regular review and development are part of the Quality Management System (QMS).
The management of ClinPack Ltd. is responsible for ensuring that all employees are aware of the quality policy, the structure and operation of the quality management system, and related tasks. To this end, we regularly review and improve the QMS, of which employee training is an essential part.