Rivarp Medical Pvt. Ltd. has a state-of-the-art production facility in Bengaluru, Karnataka. The facility is approved for manufacturing Class A, B, C, and D medical devices by the Central Drug Standard Control Organization (CDSCO).
The facility adheres to stringent quality control standards, ensuring that each product undergoes multiple quality tests before reaching healthcare professionals.
The organization is accredited with ISO 13485:2016 and ISO 9001:2015 certifications, reflecting it’s commitment to maintaining high standards of quality and safety.
Rivarp Medical Pvt Ltd., is committed to provide innovative Medical devices and equipment that meet our customer requirement, applicable regulatory and statutory requirements.
We maintain an effective quality system by managing product and process risk. The quality system is reviewed for continuing suitability by executing objectives related to:
Identifying unmet medical needs and generating innovative ideas.
Assessing the technical, clinical, and commercial viability of the idea.
Creating a functional prototype through detailed design and engineering work.
Conducting rigorous tests to ensure safety and efficacy.
Obtaining approval from relevant authorities.
Setting up production processes and quality control measures.
Monitoring the device’s performance in the real world.
At Rivarp, R&D is a complex and iterative process that drives innovation and ensures the creation of effective, safe, physician friendly & patient centric healthcare solutions.
