# Covid

**URL:** <https://ukskateforum.co.uk/t/covid/1032>\
**Category:** General\
**Created:** [April 2, 2020, 9:05pm UTC](https://ukskateforum.co.uk/t/covid/1032 "2020-04-02T21:05:53Z")\
**Posts on this page:** 1\
**Showing post:** 4807

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**Author:** ![sotonjon](https://ukskateforum.co.uk/user_avatar/ukskateforum.co.uk/sotonjon/32/20237_2.png) [@sotonjon](https://ukskateforum.co.uk/u/sotonjon)\
**Post date:** [December 7, 2021, 1:09pm UTC](https://ukskateforum.co.uk/t/covid/1032/4807 "2021-12-07T13:09:46Z")

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I’m not an expert but it is usually between 5-10 years [Vaccine Research & Development - Johns Hopkins Coronavirus Resource Center (jhu.edu)](https://coronavirus.jhu.edu/vaccines/timeline).

The MHRA was still operating under the European Medicines Agency (EU) in 2020 and issued a TUA. The mRNA vaccine was different to previous vaccines in that it used gene therapy and was a new technology. Gene therapies are usually classed as ‘advanced medicines’ and have to comply with more regulations.  
[Legal framework: Advanced therapies | European Medicines Agency (europa.eu)](https://www.ema.europa.eu/en/human-regulatory/overview/advanced-therapies/legal-framework-advanced-therapies)

However, ‘vaccines against infectious diseases’ are not classed as gene therapies under EU law: [Commission Directive 2009/120/EC of 14 September 2009 amending Directive 2001/83/EC of the European Parliament and of the Council on the Community code relating to medicinal products for human use as regards advanced therapy medicinal productsText with EEA relevance (europa.eu)](https://ec.europa.eu/health/sites/default/files/files/eudralex/vol-1/dir_2009_120/dir_2009_120_en.pdf)

So, inadvertently it created a loophole through which mRNA products could be marketed as vaccines.

The WHO called covid-19 a Public Health Emergency of International Concern (PHEIC) on March 11th allowing for vaccinations to be developed on an emergency use basis if none previously existed.

So my concern is that a new technology that only recently began trials was given a ‘TUA’ and would normally require years of trials and testing to be certified as safe.

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