Medical Device

Projipharm: expertise and compliance at the service of the medical device industry

The production of medical devices is subject to strict standards to ensure product safety, quality and compliance. Compliance with regulations such as Regulation (EU) 2017/745 (MDR) is crucial for manufacturers. These requirements mandate the implementation of robust systems at every stage of production, from design to market launch.

TAILORED SUPPORT, FROM DESIGN TO PRODUCTION

With our experience in medical device manufacturing sites, we support our clients in their projects, taking into account the specific constraints of the sector. Our expertise ensures the safety, performance and compliance of medical devices throughout their life cycle.

We work on a wide range of topics, such as:

Creating a clean room extension.
Integrating vision systems.
Modifying production flows.
Implementing a Quality Master Plan
Deploying data tracking technologies.
Validating computerised systems (VSI).
Automating production resources.

Our teams handle the various design and study phases, incorporating our in-depth knowledge of regulations and quality standards to ensure patient safety and compliance with production processes.

📢 Do you have a specific project? Projipharm Engineering is here to help you make it a reality. Talk to one of our Project Managers, and we will analyse its feasibility together and guide you with our recognised technical expertise.

Our Activities

Whether on a contract or fixed-price basis, Projipharm provides services to industrial companies. Our offering enables us to support our clients throughout the design and implementation phases.

Our expertise covers all areas of industrial production, processes, equipment and infrastructure.