BioNTech SE’s Post

We the start of this phase 2 trial, we are making further progress in strengthening our clinical portfolio. COVID-19 remains a global health threat and there is an enduring need for a vaccines that protect also the most vulnerable populations, such as the elderly and immunocompromised. We are using our clinically validated second-generation mRNA backbone to support the development of differentiated COVID-19 vaccine.

🚨 Breaking News on the Vaccine Front! 🚨 The #EuropeanMedicinesAgency (EMA) has temporarily halted its decision on the #Novavax updated #COVID19 vaccine. This #USbiotech company's unique non-#mRNA formula is making waves in the industry. Questions on its #potency and #consistency have arisen, even as the company faces a dip in #stock value. Yet, with challenges come opportunities. #Novavax is all geared up to cater to #Europe soon. 💉🌍 Stay informed, stay safe! For a deeper dive into this development, don't forget to ➡️ click on this link. ⬅️ https://lnkd.in/d-aRcwPW   #VaccineUpdate #HealthcareNews #Biotech #Pharmaceuticals #COVIDUpdates #VaccineApproval #GlobalHealth #SafetyFirst #Medicine #PharmaNews #EuropeanMarket #VaccineRace #ScienceNews #Research #HealthUpdates #MedicalInnovation #GlobalUpdates #PandemicResponse #StayInformed #HealthTech #HealthAndWellness #MedicalResearch #VaccineRollout #MarketInsights #EuropeanHealth #USHealth #VaccineInsights Spread the word! 💬🌐

Medicinal products are intended to cure or alleviate diseases and, in some cases, even prevent illness or symptoms from occurring at all. However, the use of medicinal products and vaccines can also lead to side effects. Rare and very rare adverse events can still be detected after reaching stages such as authorisation and market launch once a very large number of people have been vaccinated or treated. That is why the continuous monitoring of medicinal products carries on even after authorisation. An important component of medicinal product monitoring is the spontaneous reporting system. The Paul-Ehrlich-Institut – responsible for monitoring the safety of vaccines and biomedicines in Germany – demonstrates in the first part of its explanatory video how reporting and recording suspected side effects contributes to the safety of medicinal products. Find out more 👉 https://lnkd.in/eAFy2eSx

All of this SV40 conspiracy has been debunked so many times that it is laughable to see one reposting it… “EMA has seen no evidence of an association between mRNA vaccines and adverse events that could be linked to the presence of DNA material, nor are we aware of any scientific evidence showing that the very small amounts of residual DNA that may be present in vaccine batches could integrate into the DNA of vaccinated individuals,” the Amsterdam-based agency wrote in an emailed statement. The Food and Drug Administration, which regulates vaccines in the U.S., echoed the sentiment, saying no safety concerns about residual DNA in COVID vaccines have been identified, despite more than one billion shots being administered. “The FDA stands behind its findings of quality, safety, and efficacy for the mRNA vaccines,” the agency wrote, deferring further questions to Pfizer and other vaccine makers. Pfizer, in an emailed statement, stressed that the use of the SV40 sequence is common practice developing vaccines, including the influenza and hepatitis shots that have been administered globally for decades. “There is no evidence to support claims that the Pfizer-BioNTech COVID-19 vaccine contains plasmid DNA that could potentially impact a person’s DNA or be a theoretical cancer risk,” the company wrote, referring to DNA materials used to trigger an immune response during vaccine development. The presence of a SV40 primer within the mRNA plasmid but SV40 Promoter is not SV40 Virus. Anyone making such a claim is clearly ignorant of biotechnology. Anyone reposting of commenting on such is clearly not capable of fully understanding the difference. https://lnkd.in/ebqddtaA https://lnkd.in/eiuHtsGt

The success of the #AMC proposed by Gavi, the Vaccine Alliance to accelerate #vaccine #manufacturing in #Africa should carefully consider #regulation. The current requirement for WHO PQ as the sole regulatory pathway to guarantee quality, safety, and efficacy is not fit for purpose. Our latest Center for Global Development blog

🚀 Exciting News! MHRA Authorizes New COVID-19 Vaccine 💉 #COVIDVaccine #HealthierFuture #MHRAApproval #ScienceWins #COVID19Solution #PublicHealth #VaccineProgress #pharma #symmetrictrainings

PFIZER VACCINE CONTRACT REVEALED - Our Government has been lying to us. A South African court has ordered that the Pfizer vaccine contract between the SA Government & Pfizer be made public. And here it is : https://lnkd.in/dcaXmvvE It‘a reasonable to assumed that the terms and conditions in this contract would be very similar for every nation. Clause 5.5 provides, Purchaser (the government) further acknowledges that the long-term effects and efficacy of the Vaccine are not currently known and that there may be adverse effects of the Vaccine that are not currently known. So while poltiticans around the world were assuring the public that the vaccines were "safe & effective" - they’d signed a contract acknowledging that the long-term effects & efficacy of the Vaccine were not known and that there may be adverse effects of the Vaccine that were not known. https://lnkd.in/dtJhaPBa