The Government has rejected media reports which claim that regulatory approval for Covaxin was rushed due to “political pressure”. New Delhi:  The Government has rejected media reports which claim that regulatory approval for Covaxin was rushed due to “political pressure”. The reports claimed that Bharat Biotech, manufacturer of the indigenous... The post appeared first on .

The Government has rejected media reports which claim that regulatory approval for Covaxin was rushed due to “political pressure”. New Delhi:  The Government has rejected media reports which claim that regulatory approval for Covaxin was rushed due to “political pressure”. The reports claimed that Bharat Biotech, manufacturer of the indigenous... The post appeared first on .

The reports claimed that Bharat Biotech, manufacturer of the indigenous COVID-19 vaccine - Covaxin, "had to skip certain processes" and "speed" up clinical trials due to political pressure. The reports further claimed that there were several irregularities in the three phases of the clinical trials conducted for the vaccine.

New Delhi [India], June 28 (ANI): The Drugs Controller General of India (DCGI) has approved two doses of Pune-based Gennova Biopharmaceuticals' mRNA COVID-19 vaccine for restricted use in emergency situations for beneficiaries aged above 18 years age group.

New Delhi [India], April 22 (ANI): The Subject Expert Committee (SEC) of the Drug Controller General of India (DCGI) has asked Bharat Biotech for additional data on its COVID-19 vaccine, Covaxin, for administering it to children aged between 2-12 years, sources said.

New Delhi Feb 21 PTI The Drugs Controller General of India has granted restricted emergency use authorisation EUA to Biological Es COVID-19 vaccine Corbevax for the 12 to 18 years age group subject to certain conditions official sources said on MondayHowever the government has not taken a decision yet on vaccinating those aged below 15 yearsThe health ministry recently had said additional need for vaccination and inclusion of population for vaccination is examined constantlyThe DCGIs approval comes after the Subject Expert Committee on COVID-19 of the CDSCO on February 14 recommended granting restricted EUA to Corbevax for the 12 to 18 years age group after deliberating on Biological Es applicationThe Drugs Controller General of India DCGI had approved Corbevax which is Indias first indigenously developed RBD protein sub-unit vaccine against COVID-19 for restricted use in emergency situations in adults on December 28It has not been included in the countrys vaccination drive The DCGI on Monday granted restricted EUA to Corbevax for the 12 to less than 18 years age group subject to certain conditions an official source saidIn an application sent to the DCGI on February 9 Srinivas Kosaraju the head of quality and regulatory affairs at Biological E Limited had said the firm had received approval for conducting phase 23 clinical study of Corbevax among children and adolescents aged 5-18 years in SeptemberBased on the no-objection certificate Biological E has initiated the clinical study in October 2021 and has evaluated the available safety and immunogenicity results of the ongoing phase 23 study which indicated that the vaccine is safe and immunogenicThe proposed application is for obtaining permission for restricted use in an emergency situation in adolescents aged 12 to less than 18 years based on interim results of the ongoing phase 23 clinical study considering the current pandemic and widespread of COVID-19 vaccine in India Kosaraju had said in the applicationThe Corbevax vaccine is administered through the intramuscular route with two doses scheduled 28 days apart and is stored at two to eight degrees Celsius temperatures and presented as 05 ml single dose and 5 ml 10 doses vial packAccording to the health ministry the company has conducted phase 12 and 23 clinical trials of its COVID-19 vaccine in the countryFurther it has conducted a phase 3 active comparator clinical trial to evaluate superiority against Covishield vaccine it said PTI PLB ANB ANB

New Delhi [India], January 12 (ANI): Antiviral drug Molnupiravir is not included in the National treatment task force for COVID-19, said Director General, Indian Council of Medical Research (ICMR) Balram Bhargava on Wednesday.

New Delhi [India], December 29 (ANI): The Drug Controller General of India (DCGI) has given approval to the Hyderbad-based pharmaceutical company Biological E to conduct phase 3 clinical trials of its COVID-19 vaccine Corbevax as a booster dose, said sources.

Hyderabad (Telangana) [India], December 28 (ANI/PNN): Hyderabad, Optimus Pharma announced launching of their front line COVID-19 medication Molnupiravir in the Indian market, as they have received permission the restricted emergency use for Covid-19 drug.

New Delhi Dec 25 PTI The Drugs Controller General of India DCGI has granted emergency use authorisation to Bharat Biotechs Covaxin for children above 12 years with certain conditions sources saidon SaturdayThe Subject Expert Committee on COVID-19of the CDSCO on October 12 after deliberating Bharat Biotechs EUA application had recommended granting emergency use approval to Covaxin for use in the 12-18 years age group with certain conditionsThe recommendations of the SEC were evaluated by another experts committee after which DCGI had sought additional data from the firm a source saidThe DCGI gave its approval Friday the source said PTI PLB ZMN