‘Who (what) is EU Notified Body Med19/#avct cld be working with’ to obtain EU IVD self use CE certificate. What EU state cld they be from, is it coincidental they are located in Spain, same city hospital area avacta used to verify AffiDX lft, Med19 have a Spainish website
1/15
On EU NANDO database from 18 Notified Bodies (NB) Med19/#avct could be working with ‘AEMPS Notified Body’ who certify med product devices under EU directive 98/79/EC for self use in-vitro diagnostic test (IVD). If not, then 17 other EU Notified Bodies to work with
2/15
EU Notified Body much like mhra/fda. AEMPS NB is located in Spain/Madrid/Delgado. Same country, city, hospital area #avct used to independently verify AffiDX. AEMPS CE certified AffiDX for professional use, was application for AffiDX CE self use submitted around same time.
3/16
Both EU Notified Body & hospital used to independently verify AffiDX are max 5/6 miles from one another. Google map shows location distance. Think this isn’t a coincidence, has Med19 planned to validate lft in Spain. Cld be why AS said Med19 doing superb job in Q&A
All 18 Notified Bodies are accredited by EU, robustly checked for compliance and adhere to EU special directive 98/79/EC for IVD self use, and certify them. Notified Body/manufax requirements & scope of works in pics
Cont from post 5/15: Notified Body/manufax requirements & scope of works in pics, Is not exhaustive to list but can be much wider. Tweet 5-6 pics from EU commission doc 2021. Question & answers on how to obtain CE mark and certificate for #covid19 IVD LFT for self use
EU Notified body: Agencia Española de Medicamentos y Productos Sanitarios (AEMPS) from Spain Madrid is one of 18 listed EU accredited Notified Bodies, who are on EU commissions NB Nando site. PDF shows scope to CE certify IVD for self use under EU 98/79/EC Directive
Wld be logical/easier for Med19 to use EU Notified Body in Spain Madrid. This only applies if Med19 submitted application before or on 25/05/21, after this date new 2017/746 regs apply. Med19 not applied by 25/05/21 they wld take IVDR 2017/746 route to CE mark AffiDX
Even if EU notified body AEMPS isn’t working with Med19 & #avct there is 17 others that can do same work. Med19 can only use one from EU 18 list. Spain hospital, Spain notified body, Med19 Spain website would be the perfect plan to obtain CE IVD self use certificate in EU
9/15
Tweets 1-9 apply if application for EU CE IVDD self use was before or on 25/05/21. If after 25 May then new regs IVDR EU 2017/746 apply. EU NANDO data base show only 6 Notified Bodies on list who certify under new regs IVDR EU 2017/746, Med19/#avct are using one of them
10/15
Med19 conducted submitted lay user study forming part of application to Notified Body on ease of use by non-professional (lay user) Going by medrxiv report which #avct did with Spain hospice users were non-professional. Med19 wld hav same trial success for self use CE mark
11/15
Almost certain UK MHRA will follow IVDR regs 217/746. Keeps UK aligned with EU, basically makes MHRA job easier. The fact regs 217/746 is robust in assessment of IVD tests, means EU Notified Bodies will have done all the hard work. EU/CE mark carries weight globally
IVDR EU regulation 217/746 would be the best route. Receiving CE mark for self use under this default regulation will in-force 217/746 into all 27 EU states, regardless of individual states own policy & laws regarding in-vitro diagnostic (IVD) tests for self use
Which ever route taken AS is determined 2 get EU CE for self use. He shld be, why!? because it opens up global markets for #avct AffiDX “Lets not forget CE Mark has been historically the passport for approval in majority of international markets” Gold pass 2 global markets 14/15
And looks like EU CE mark certificate for home use is finally granted. No more waiting, second guessing, what ifs any more Med19 #avct find themselves in a unique position to take lion share of self use market. Certain they will do and smash it @downunderfutbol👇👌👍🙂15/15
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Mologic CE marked AffiDX for professional use, CE mark with #avct not Med19 AffiDX solely an avct brand. Med19 CE self use mark for Meduflow, EU CE mark solely Med19’s for Meduflow not avct. Professional & self use CE marks differ in use, both need separate CE marks.
1/23
Med19 have done all the hard work re: lay user study, filing all docs for CE mark for self use with EU notified body, as well as the money and time spent in obtaining CE self use mark for Meduflow. Med19 will be looking to keep and make a serious return on their investment
2/23
I suspect main points under license agreement between #avct Med19 would be:- use Affimer IP in Meduflow, Med19 achieve minimum yearly sale targets, which global territories (if not covering all world), royalty % per test sold, duration of license agreement,
#AVCT Spoke to someone at Med19 today for 1hr 46min. Not give any detailed info. Wat I will say is: HUA in very final stages, infact very little else to do. Everything asked for has been submitted, even if EU asked for it twice its been given (if u understand wat Im implying) 1/9
Global demand is huge, getting calls from global govs/busi/high caliber distributors-business men. Med19 have orders, ready to take more orders soon as HUA is given. Affidx recognized as a gold standard reliable test, easy to use. Med19 working with global distributors 2/9
Med19 ready 2 scale up and sell multiple millions of lft’s, for global busi/gov/consumer orders. All Affidx components in stock for first batch orders. Product box/packaging/art work/instructions for consumer use almost ready, proof readin sign off needed by EU HUA body 3/9