Apr 23, 2021
The ISO 13485 standard is essential in the medical product industry, enabling the creation of standardized rules for all agents that play a part in the supply chain, on top of domestic regulations. We analyze what ISO 13485 is, the benefits of implementing it and its... 
Oct 26, 2020
Sterilized medical device packaging must guarantee that the contents within will remain sterile throughout the entire lifecycle of the product – from the moment it leaves the factory until the final consumer opens it to use it. The ISO 11607 standard addresses this... 
Apr 21, 2020
The ISO 17025 accreditation outlines a series of protocols required to accredit the technical capabilities and quality standards of a testing and calibration laboratory. This ISO certification therefore evidences the capability of a laboratory to consistently provide... This website uses cookies to improve your experience. We'll assume you're ok with this, but you can opt-out if you wish.Accept Privacy & Cookies Policy
