The UK has paid £ 1.5 million for a computer program called ‘AL’ to track or trace all the adverse reactions that COVID19 vaccines will produce.
Why the UK government paid a high price for this program or software?
Is the British Government Really Expecting a High Volume of Adverse Drug Reactions from the vaccines for COVID19?
Please, PAY ATTENTION to this CONTRACT, includes important information that we need to understand
Here we have some parts of the contract that the MHRA (Medicines & Healthcare products Regulatory Agency):
Type of the contracting authority: “Ministry or any other national or federal authority, including their regional or local subdivisionsI.”
Main activity: Health.
Short description: “The MHRA urgently seeks an Artificial Intelligence (AI) software tool to process the expected high volume of Covid-19 vaccine Adverse Drug Reaction (ADRs) and ensure that no details from the ADRs’ reaction text are missed.”
Description of the procurement: The MHRA urgently seeks an Artificial Intelligence (AI) software tool to process the expected high volume of Covid-19 vaccine Adverse Drug Reaction (ADRs) and ensure that no details from the ADRs’ reaction text are missed.
Type of procedure: Award of a contract without prior publication of a call for competition in the Official Journal of the European Union in the cases listed below.
The procurement falls outside the scope of application of the directive
“For reasons of extreme urgency under Regulation 32(2)(c) related to the release of a Covid-19 vaccine MHRA have accelerated the sourcing and implementation of a vaccine specific AI tool.
Strictly necessary — it is not possible to retrofit the MHRA’s legacy systems to handle the volume of ADRs (Adverse Drug Reaction) that will be generated by a Covid-19 vaccine. Therefore, if the MHRA does not implement the AI tool, it will be unable to process these ADRs effectively. This will hinder its ability to rapidly identify any potential safety issues with the Covid-19 vaccine and represents a direct threat to patient life and public health.
Reasons of extreme urgency — the MHRA recognises that its planned procurement process for the SafetyConnect programme, including the AI tool, would not have concluded by vaccine launch. Leading to a inability to effectively monitor adverse reactions to a Covid-19 vaccine. Events unforeseeable — the Covid-19 crisis is novel and developments in the search of a Covid-19 vaccine have not followed any predictable pattern so far.”
At least it is recognised, indirectly, that nobody knows the adverse effects of the vaccines for COVID will have on human beings. According to the scientific standards, we need at least 10 years to approve a drug or vaccine to be used in human beings with safety, but we are going beyond these fundamental principles of research and application of drugs and vaccines. Who knows what consequences it will take.
I would not like to be a guinea pig, I do not know about you.
Here is the link where you can read this News:
Click here: UK to use AI for COVID-19 vaccine side effects
Link for the Company website with the official contract with the UK government to buy the “AL” software, you can read by yourself the contract made: United Kingdom-London: Software package and information system 2020/S 207-506291 Contract award notice
Link to MHRA website: MHRA (Medicines & Healthcare products