SpOvum has received the ISO 13485 certificate. This certificate was issued by TUV SUD.
What you should know regarding ISO 13485
What is a medical device?
A product that is designed for use in the diagnosis, prevention, and treatment of illnesses or other medical disorders is known as a medical device. Examples include instruments, machines, implants, and in vitro reagents.
Whom does ISO 13485 serve?
Organizations engaged in the design, production, installation, and maintenance of medical devices and related services are intended users of ISO 13485. Additionally, it can be utilized by internal and outside parties, including certification organizations, to support their auditing procedures.
Compliance with ISO 13485
Like other ISO management system standards, ISO 13485 does not mandate certification, and firms can still adopt the standard and enjoy many benefits without going through the certification process. However, third-party certification can show regulators that you have complied with the standard’s requirements. The ISO doesn’t carry out certification
This is reinforcing SpOvum’s commitment to the adoption of best practices in Quality Management towards continual improvement.
In this regard SpOvum thanks Mr. S L Sriram for his guidance all along, in achieving this milestone.
With SpOvum as your partner, you can be assured of the best practices in the industry!