decision on whether to appoint a special master to review documents seized during the fbi search at mar-a-lago. this hearing comes after president trump s lawyers responded to the d.o.j. damning filing on tuesday. in their response, trump s lawyers pressed their argument that an independent review is needed. despite the justice department saying it had already filtered out any privileged documents. trump s lawyers acknowledge that classified material was found at mar-a-lago. but say there was no need to be alarmed. that trump s home should never have been searched for this. while we still don t know what was in the 320-plus highly classified documents that were recovered, we do know, trump attempted to obstruct the fbi s investigation into the handling of classified material. there s a lot to digest. let s go to west palm beach, florida, outside of the courthouse. the hear willing start at 1:00 eastern time today. walk us through what plays out now. about three hours from
conceal those documents. i have to say, the question that people were asking me all day after this, what in the world was he doing with over 300 pages of classified documents at mar-a-lago? after he s left office? is he going to use it for wallpaper there. is he going to show it to friends and family who dined with him? why should an ex-president of the united states have sensitive classified documents like this in unsecured areas of his personal residence? that s an answer i think maybe we ll see when we have a hearing later today. you re a former cia intelligence officer. you understand the classifications and the different levels. some documents we saw were near the top of the classification list. the trump legal team argued in this filing last night, quote, simply put, the notion that
Tuesday, January 12, 2021
This year has been perhaps the most significant year for medical device companies from a regulation perspective since the Medical Device Rules, 2017 (explained below) came into force on January 01, 2018. The Government has amended medical device regulation to significantly expand the reach of medical device regulation. There is also some discussion on enacting a new legislation altogether specifically for medical devices (medical devices are currently regulated as drugs). The sector has also been largely unaffected by the COVID-19 pandemic and the regulator provided for relaxations in regulatory compliances as required.
In this wrap, we have covered some of the significant developments in the medical device space this year and what we hope to see ahead in 2021.