18 - 19 February, 2020 | Berlin, Germany
Contact Us: 44 (0) 207 368 9300
Werner Kexel discusses the 3rd revision to the standards guideline 60601 and tips for medical device manufacturers on how to prepare for the changes!
Please note: That all fields marked with an asterisk (*) are required.
*Processing your payment may take a moment. Please click submit payment only once, and do not refresh this page. Doing so may result in your credit card being charged more than once.