
Re accodification (sure that isn't the process of adding cod to a dish?), should we be thinking about referencing various legislative sources from our model text in parameterized fashion, if possible, as we make our clauses jurisdiction-specific? *Eve Maler*Cell +1 425.345.6756 | Skype: xmlgrrl | Twitter: @xmlgrrl On Fri, Jan 15, 2016 at 12:48 PM, James Hazard <james.g.hazard@gmail.com> wrote:
This is very interesting and I agree.
I had accodified ( Eve ;) ) the European text so that one can rehash it and make deep links into it. E.g.:
My sense is that such requirements can drive adoption of good (even best) practices, for instance regarding retention and access:
Those requirements could be baked into agreements with users and governments, such as Appendix 2 to the "Model Clauses" (the tan-colored part near the end of the document):
http://www.commonaccord.org/index.php?action=doc&file=Dx/Acme_UK/01-EU-US-DataTransfer/Doc_v0.md
On Thu, Jan 14, 2016 at 3:13 PM, Adrian Gropper <agropper@healthurl.com> wrote:
In the last month two very important regulatory guidance documents have been released by the EU and US governments respectively:
http://europa.eu/rapid/press-release_MEMO-15-6385_en.htm and
http://www.hhs.gov/hipaa/for-professionals/privacy/guidance/access/index.htm...
By adding to these regulations a single constraint - that an individual can own and specify the UMA Authorization Server if they choose to - I think we can derive a complete UMA Legal profile and associated clauses.
I've started analysis of the US reg at http://bit.ly/HEARTfromHIPAA I think a similar analysis could be interesting for the EU regs.
Adrian
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Adrian Gropper MD
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