We are thrilled to announce that Opharmic Technology (Opharmic) has successfully obtained the prestigious ISO 13485:2016 certification, validating our commitment to maintaining a robust quality management system. This achievement highlights our dedication to designing and developing cutting-edge ultrasound systems in the MedTech industry while adhering to the highest standards.
ISO 13485:2016 certification holds global recognition as a benchmark for quality and safety within the medical device sector. It provides a structured framework that meticulously aligns medical device design, development, and production with exacting customer specifications and stringent regulatory requirements.
This esteemed certification demonstrates our preparedness to serve our valued partners by staying abreast of the latest regulatory requirements specific to the medical device industry. Opharmic has successfully completed the certification process, which commenced with the development of our corporate quality policy, “Quality is a HABIT.” This policy underpins our commitment to ensuring that our solutions are perfectly attuned to every aspect of healthcare.
Attaining the ISO 13485:2016 certification represents a significant milestone in our pursuit of excellence. It signifies our unwavering dedication to delivering safe and high-quality ultrasound systems and services that not only meet the needs of our partners but also comply with the most rigorous industry standards.
Our partners can confidently choose Opharmic as their trusted ally for all their ultrasound system application development, knowing that they are aligned with a company wholly dedicated to excellence in every aspect of our work.