BELARUS CHILDREN ARE USED FOR CLINICAL TRIALS OF VACCINES (PART II)

in #vaccination6 years ago

This story is an epic fail!
And the price of it was a life of a newborn baby...

The first part is here

As we've already discovered in the 1st part, the Korean representatives had a fake certificate about finished trials of this vaccine in 2014.
Later it was discovered that in a year, in 2015, the trials were still being held in Philipines and in China.

And if they really were finished that year, in 2015, then the Korean company had to get the registration for a new vaccine, but they did NOT!

Why?

Maybe because trials showed negative results?!

Just the same was in the USA. The vaccine was tested, but it is still NOT registered there, so again - what was wrong with those tests??

However, unlike Belarus, in all these countries, the tests were conducted exclusively on volunteers who were paid a lot of money and who were under constant supervision of doctors.

The Ministry of Health in Belarus repeat about safety of the vaccine that was used in 43 countries.
Sounds great, but why it is NOT registered anywhere in the world?! Even in the country that has produced it!!

When an unregistered drug is purchased, additional requirements are applied to it.
The Ministry of Health in Belarus says it should be "registered in the ICH countries (International Conference on Harmonization of Technical Requirements for the Registration of Medicinal Products for Humans) .
The list includes countries with a strong registration regulatory authority (EU countries, USA, Canada, Japan, Switzerland , South Korea, etc.) ".

For those who have never come across this industry, the explanation sounds pretty convincing, BUT the investigators of this scandal story asked the providers of drugs about this organisation, and they just were laughing!

ICH does not include any country in the world!
There are no intercountry agreements and commitments in activity of ICH, as there is no mutual recognition of registration of medicines.

This is just an association of the most diverse organizations from a number of countries. And there are NO members from Belarus in it at all!

The purpose of the organization is not recognition of mutual registration, but only the development of uniform approaches to quality control of drugs.
In other words, representatives of organizations meet, exchange experience, give each other recommendations, and then leave without any obligations to each other!

So it has nothing to do with Eupenta, because it has no registration anywhere!

The law "On medicines" has no info about ICH at all, so this argument doesn't work.

The Ministry also said about the WHO prequalification that is a kind of world-class quality mark guaranteeing the quality, safety and efficacy of medicines.

But wait, again reference to this very main law Law on Medicines, where there is not a single word about the prequalification of WHO and that it allows the import of medicines without registration in Belarus!

The WHO prequalification program was established with the aim of simplifying the admission of medicines to developing countries that do not have their own structures involved in quality control of medicines. This is a list of countries such as Africa, South America, Asia, so those countries where there is an unfavorable epidemiological situation.

Unlike the testing and registration of medicines in developed countries, WHO prequalification is carried out by a simplified procedure: only the 1st stage of experiments are needed, sometimes even NO trials are held at all!

Many world companies use this rule to enter their new medicines and vaccines into the coutnry and test it on people! And it's absolutely free!

Trillions of dollars are saved!
Even if there are problems, nobody will notice them, because the level of mortality in these countries are extremely high.

A perfect scheme...

SO Why should the EU, the USA, Belarus, Russia and other developed member countries of WHO spend millions on checking and registering medicines when there is such a "world-class quality mark" as prequalification?

The answer is simple - because they perfectly know the difference between their country and, for example, Nigeria, Congo or Somalia. Neither in the US, nor in the EU, nor in Russia there are no requirements for registration of medicines to provide prequalification of WHO, but there is a requirement to provide registration in the producing country and with the mandatory passage of the three phases of clinical trials!

No country demands the prequalification documents when a new vaccine enters the country.

Why?

Because they mean just nothing!

And now the MInistry of Health use this argument to hide their corruptive outrage?!

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Keep steeming for a better tomorrow.
@Acknowledgement - God Bless

Posted using https://Steeming.com condenser site.

ой, жуть какая(
вот так вот и верят люди "экспертам" с зомбо-ящиков на слово... сами не разобравшись в таком важном вопросе, эх...

I cannot imagine the pain those parents are feeling right now :'(

Кто-то нажился на смерти других. Самое обидное, что пострадали самые безобидные - дети.

Nice read. I leave an upvote for this article thumbsup

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