Lessons from the Lab
This eBook, created in partnership with Medical Products Outsourcing Magazine, addresses common challenges and best practices for...
This eBook, created in partnership with Medical Products Outsourcing Magazine, addresses common challenges and best practices for...
The release of ISO 10993-1 in 2018 marked a significant shift in the biocompatibility evaluation of medical...
This comprehensive eBook serves as an essential guide for professionals involved in the design and manufacture of...
Manufacturers are required to perform a biological evaluation of any medical device as outlined in ISO 10993-1....
Disposable plastic components are increasingly popular in biopharmaceutical drug manufacturing systems due to their cost-effectiveness and reduced...
In this episode, host Brandon Miller is joined by Dr. Matthew Jorgensen and Dr. Helin Räägel. Dr....
In this episode of the RCA Podcast, host Brandon Miller is joined by Dr. Matthew Jorgensen and...
Cytotoxicity testing is a critical endpoint for all medical devices that come into contact with patients or...
The submission process to the FDA can be a stressful and uncertain time for a medical device...
Change management in the design of medical devices is a critical process, frequently highlighted in FDA 483...