Close
Achema middle east
swop processing & packaging

BioNTech And Regulator Differ On COVID Jab Approval- WAS

Note* - All images used are for editorial and illustrative purposes only and may not originate from the original news provider or associated company.

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

– Access the Media Pack Now

– Book a Conference Call

– Leave Message for Us to Get Back

Related stories

Russia, Vietnam Collaborate on Biopharma Technology Transfer

Russia and Vietnam have gone on to officially formalize...

Trump Order to Go Heavy on D2C Pharmaceutical Ads

US President Donald Trump is all set to order...

Is US Planning Executive Order on Chinese Pharma Companies?

It is worth noting that the pharmaceutical sector’s recent...

The Realities of the Nursing Shortage in Rural America

Along with multiple public health crises, the United States...

According to a story in the Welt Am Sonntag (WAS) newspaper, the launch of the vaccine developed by German pharmaceutical company BioNTech for the Omicron coronavirus type may be postponed because of a dispute with the regulator over the licencing procedure. 

Ugur Sahin, the chief executive of BioNTech, does not intend to submit any more clinical trials, WAS said, citing the Financial Times. However, the regulator should still determine by the end of June whether or not to authorise the new vaccine.

According to Sahin, who was quoted by WAS, the rationale for this was that the new COVID-19 vaccine could be given in three months if the approval “should go through the same regulatory process as other flu vaccinations.”

Klaus Cichutek, the director of the Paul Ehrlich Institute (PEI), the German medical watchdog, told the newspaper that there was no justification to take a chance by skipping the regular regulatory procedure while making arrangements for the upcoming pandemic wave.

The PEI chief informed WAS that “Mr. Sahin insists that only animal evidence be given for approval of alternative vaccinations,” adding that while this may be done in an emergency, there was none at the time.

Vaccine manufacturers may be granted first licences for improved COVID-19 vaccinations in September, as per PEI and the European Medicines Agency (EMA), if the vaccine manufacturers demonstrate in human trials that they are superior to current vaccines.

Latest stories

Related stories

Russia, Vietnam Collaborate on Biopharma Technology Transfer

Russia and Vietnam have gone on to officially formalize...

Trump Order to Go Heavy on D2C Pharmaceutical Ads

US President Donald Trump is all set to order...

Is US Planning Executive Order on Chinese Pharma Companies?

It is worth noting that the pharmaceutical sector’s recent...

The Realities of the Nursing Shortage in Rural America

Along with multiple public health crises, the United States...

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

– Access theMedia Pack Now

– Book a Conference Call

– Leave Message for Us to Get Back

Translate »