This posts discusses BSI’s article on the status of the draft ISO 13485:201X standard. Recently BSI published an e-newsletter and in it was an excellent article explaining the status of the next draft revision of ISO 13485 and some of
Update to BSI White Paper on Proposed EU Regulations for Medical Devices & IVD’s
BSI recently updated the white paper on Proposed EU Regulations for Medical Devices & IVD’s to reflect the latest EU vote in early April, enabling the commission to move forward with the legislation.
BSI White Paper on Proposed EU Regulations for Medical Devices & IVD’s
This article focuses on BSI’s new White Paper Series for the Medical Devices & IVD’s industries, First one on the EU Proposed Regulations 9 April 2014 – Today marks the beginning of a series of white papers that BSI has
TÜV SÜD & Global EMC IEC 60601-1, 3rd ed Seminar
TÜV SÜD Canada & Global EMC will be giving an all day seminar on IEC 60601-1, 3rd ed. on Feb 21, 2014 in the Montreal, Canada area for a very reasonable cost of $100. This will be on the test
RAPS & Medicaldeviceslegal.com EU Medical Devices Regulation Chart
This Regulation Chart & the blog post contents is Thx to Medicaldeviceslegal.com and the RAPS Dutch/Flanders chapter. We are grateful to them for sharing such a valuable tool and hope you get a lot of good use from it too. All they