Having written in the last year a widely discussed paper about Informed Consent the new WMA revision #25 makes this rather waste paper:
For medical research using identifiable human material or data, physicians must normally seek consent for the collection, analysis, storage and/or reuse. There may be situations where consent would be impossible or impractical to obtain for such research or would pose a threat to the validity of the research. In such situations the research may be done only after consideration and approval of a research ethics committee.
With this paragraph in effect you can now to do every test on every sample that you possess. I will tell you from my practical experience how this work Continue reading Seoul update of the WMA declaration – you lost your rights


