BEVER Medical offers end-to-end medical device development services, from initial design to full-scale manufacturing. Our comprehensive approach, advanced facilities, and commitment to quality ensure that your medical device is developed efficiently, and in compliance with all regulatory standards.
Our team will provide five development services to our partners
Our design phase is driven by innovation and precision. We work closely with you to understand your vision and requirements, providing creative and technical input to shape your medical device. This collaborative process ensures that the final design not only meets functional and aesthetic standards but also meets user needs and market demands.
Prototyping
Prototyping
Prototyping is a crucial step where ideas take tangible form. Utilizing advanced manufacturing technologies, we create accurate prototypes that allow for thorough evaluation and refinement. This iterative process helps in identifying potential improvements and ensures that the design is both feasible and manufacturable.
Verification and Validation Testing
Verification and Validation Testing
Our verification and validation (V&V) testing processes are designed to ensure that your medical device meets all necessary performance and safety standards. We conduct rigorous testing of products, materials, and packaging to comply with ISO and FDA standards. This comprehensive testing regime helps mitigate risks and ensures that the device functions as intended under real-world conditions.
Pilot Production
Pilot Production
Before moving to full-scale manufacturing, we offer pilot production services. This phase allows for the small-scale production of your device to further refine the manufacturing process and identify any issues that may arise. It serves as a bridge between development and full-scale production, ensuring a smooth transition.
Manufacturing Partner
Manufacturing Partner
BEVER Medical is not just a development partner but also a capable manufacturing partner. Our facilities are equipped with state-of-the-art equipment, capable of handling full-scale production. We ensure that every device is manufactured to the highest quality standards, maintaining consistency and reliability across batches.
Creative and technical inputs for your medical device
Selecting the appropriate materials for the design
Testing of products, materials, and packaging to ISO or FDA standards
Writing documentation and offering support for regulatory submissions
Medical Murray's development process and documentation comply with FDA 21 CFR Part 820, as implemented through our ISO 13485:2016 Certified Quality System.