Cevidra is committed to implementing quality processes to ensure the satisfaction of all stakeholders from the MAH to patients.
To comply with all the regulatory requirements applicable on the French market and/or on other sales markets concerning the services and products managed by CEVIDRA, and to comply with the requirements formulated in the contracts signed with our partners.
Commitment to continuous improvement of the quality of products and services and therefore continuous improvement of all CEVIDRA processes. This continuous improvement must ensure an overall performance in line with Cevidra’s quality objectives and with the explicit and implicit requirements and needs of all our stakeholders.
Respect for personal data (GDPR Policy):
Cevidra has established a specific procedure for the processing and protection of personal data, in compliance with the Regulation (EU) 2016/679 of the European Parliament and of the Council of 27 April 2016 on the protection of individuals with regard to the processing of personal data and on the free movement of such data.
Our Data protection officer (DPO) is the guarantor of the proper implementation of these processes. If you have any questions or requests regarding your personal data, you can contact us at the following address : email@example.com.
As a pharmaceutical company:
Cevidra is a committed and trusted partner. We provide tailor-made services to develop long term partnerships with our clients and all our activities are conducted in accordance with GDP & GMP standards. Our authorizations are periodically renewed by the French Health Authority (ANSM).