CERTIFIED QUALITY MANAGEMENT
Provepharm ensures the quality of its products through a Quality Management System (QMS)
Medical devices<p>Our Quality Management System is ISO 13485 certified</p>
Drugs<p>Our activities comply with applicable Good Manufacturing Practices and Good Distribution Practices</p>
Active substances (API)<p>Our activities comply with Good Manufacturing Practices (Part 2)</p>
A QUALITY POLICY BASED ON 5 STRATEGIC PILLARS
Provepharm asserts itself as an independent French international pharmaceutical player whose mission is to innovate to realize the full potential of each molecule. This is to provide treatments that help improve patients' lives.
With its skills in chemistry and pharmacy, Provepharm develops and markets a range of safe, effective and quality health products, and also offers development and manufacturing services in fine chemistry and peptide synthesis. The quality policy, linked to our business project through a shared culture, is based on the values of commitment, integrity and audacity.
This policy is broken down into our 5 strategic pillars.
A CERTIFICATION PROCESS AT THE MEDICAL VISIT
Since July 2022, Provepharm SAS has been certified for its information activity by canvassing or prospecting aimed at promoting medicines, in accordance with the HAS certification reference system of March 2017.
In accordance with the promotional information charter (in French only) by canvassing or prospecting aimed at promoting medicines drafted by the French National Authority for Health, Provepharm has set up a promotional information activity fully integrated into our Quality Management System.
Thus, through this policy, we confirm our commitment to promote the proper use of our medicines among healthcare professionals, and to include our promotional information actions in a process of continuous improvement.
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