Is the EMA about to fully approve the vaxxines so that they can be mandated and everyone force-vaccinated?

Is the EMA about to fully approve the vaxxines so that they can be mandated and everyone force-vaccinated?

A claim has been made that in Europe the pharmaceutical companies did not renew their request for a conditional marketing authorisation (CMA) and that therefore the Covid vaccines are no longer approved for use. According to a French article, they were supposed to do so six months in advance of the expiration of the one-year temporary conditional marketing authorisation. I have checked the cited EU regulations and this is correct (https://ec.europa.eu/health/sites/default/files/files/eudralex/vol-1/reg_2004_726/reg_2004_726_en.pdf):

6. In exceptional circumstances and on public health grounds the
Commission may grant exemptions from paragraphs 4 and 5. Such
exemptions must be duly justified.
7. Following consultation with the applicant, an authorisation may be
granted subject to certain specific obligations, to be reviewed annually
by the Agency. The list of these obligations shall be made publicly
accessible.
By way of derogation from paragraph 1, such authorisation shall be
valid for one year, on a renewable basis.

COMMISSION REGULATION (EC) No 507/2006
of 29 March 2006 (https://ec.europa.eu/health/sites/default/files/files/eudralex/vol-1/reg_2006_507/reg_2006_507_en.pdf):

(9) In accordance with Regulation (EC) No 726/2004, conditional marketing authorisations will be valid for one year
on a renewable basis. The deadline for submission of a
renewal application should be six months prior to the
expiry of the marketing authorisation, and the opinion of
the European Medicines Agency (hereinafter the Agency)
on the application should be adopted within 90 days of
its receipt. To ensure that medicinal products are not
removed from the market except for reasons related to
public health, the conditional marketing authorisation
should, as long as a renewal application is submitted
within the deadline, remain valid until the Commission
reaches a decision based on the renewal assessment
procedure.

According to my data, the vaccines will not reach the end of their one-year conditional marketing authorisation period until this December, and the following January and March so I don’t see a justification for the claims made in both France and Italy (https://forlifeonearth.weebly.com/insights-into-the-european-public-data-on-cmas-30321.html):

The article originating in Italy claims that the conditional marketing authorisation is no longer valid but the author does not provide the proof: In Italy The Vaxx Is No Longer Legally Approved For Use: https://www.fromrome.info/2021/08/16/in-italy-the-vaxx-is-no-longer-legally-approved-for-use/:

… That Conditional Approval for Commercial use authorization has expired, in law, with the official recognition by AIFA, the Italian Pharmaceutical Approval Agency, of the use of other monoclonial anti-bodies as an effective cure for SarsCov19 infection. …

In France, it is Dr. Philippe Chazournes who has said that the conditional marketing authorisation is no longer valid (https://qactus.fr/2021/08/20/urgent-le-docteur-philippe-de-chazourne-nous-lache-une-bombe-et-nous-explique-par-preuves-que-les-labos-nont-pas-renouvele-leur-autorisation/) and:

Statement by Philippe de Chazournes 14.8.21.png

However, as stated above in EU regulation 507/2006
of 29 March 2006, “the conditional marketing authorisation
should, as long as a renewal application is submitted
within the deadline, remain valid”. So it seems to me that we have an anomalous situation here, in which, if the pharmaceutical companies have indeed failed to submit an application to renew, we do not know if the CMA remains valid or not. It would seem to depend on the choice of action of the European Medicines Agency (EMA). Britain, of course, after Brexit, is not part of this but nevertheless seems to follow suit with the actions of the European Union.

Given that we are in a situation of extreme uncertainty and deep suspicion of “authorities” by the general public after the abuse perpetrated on them in the last 18 months, there is, of course, another interpretation to be put on all of this. Could it be that the pharmaceutical companies effectively control the EMA and that they knew from the outset that the EMA would automatically grant them an unconditional marketing authorisation after a certain time? Despite the fact that 34,052 Covid-19 injection-related deaths and over 5.46 million injuries in EU/UK/US had been reported as at 1.8.2021 (https://blog.nomorefakenews.com/2021/08/17/massive-fraud-in-reporting-vaccine-injuries-withheld-data-pretense-of-safe/) and that it is universally acknowledged that the voluntary or “passive” reporting systems under-report vaccine adverse events by up to 100 times, such that the real number of deaths could be 3.5 million or more, they are going to give full approval for marketing authorisation shortly so that the vaccines can be mandated? This despite the fact that the deadlines for submitting confirmation of efficacy, safety and tolerability of the vaccines are between a year and three years away (https://forlifeonearth.weebly.com/insights-into-the-european-public-data-on-cmas-30321.html):