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WHO PREQUALIFICATION
620% rally makes Cupid the costliest stock in its category at 197 P/E. Should investors be cautious?Cupid, a contraceptives manufacturer, has seen a remarkable 620% rally in the past year, making it the costliest stock in its category with...- Biological E receives phase II WHO pre-qualification for oral polio vaccineBiological E Limited is celebrating a groundbreaking moment! The World Health Organization has officially granted phase II pre-qualificatio...
- Zydus gets WHO nod for its typhoid vaccineZydus Lifesciences Ltd has received in-principle approval from the WHO for its Typhoid Vi conjugate vaccine, ZyVac TCV. Eligible for UN pro...
- WHO clears Bavarian Nordic's vaccine as first shot against mpoxThe World Health Organization has approved Bavarian Nordic's mpox vaccine, the first to be cleared for use in African countries affected by...
- Serum Institute's multivalent meningococcal meningitis vaccine gets WHO prequalificationThe Serum Institute of India (SII), world's largest vaccine maker by volumes on Wednesday said its vaccine to protect against the five pred...
- Hetero's oral drug gets WHO PrequalificationIt is the first prequalification for a generic version of Pfizer's Covid-19 oral antiviral drug paxlovid, the company said. The WHO made a ...
- Hetero gets WHO prequalification for generic Covid antiviral PaxlovidThis is the first WHO prequalification for Paxlovid - a combination of nirmatrelvir and ritonavir which is recommended for treating mild an...
- Bharat Biotech's Rotavac 5D receives WHO PrequalificationThe new variant of Rotavac, Rotavac 5D, is a unique rotavirus vaccine formulation that can be administered without a buffer and its low dos...
- Process to receive WHO pre-qualification for Covaxin on: GovtIn response to a question on when the WHO approval for Covaxin is expected, the minister said the data required for approval was submitted ...
- WHO asks Serum Institute of India for Covishield trial data to begin global supplySerum Institute of India is one of the manufacturers that has signed up to supply up to 400 million doses of vaccines to the Covax Facility...
- Russia submits application to WHO for accelerated registration, prequalification of Sputnik V vaccineThe Prequalification of Medicines Programme is a United Nations programme managed by WHO. It is the only global medicines quality assurance...
- World Health Organization says discussing new COVID-19 vaccine with RussiaPresident Vladimir Putin said on Tuesday that Russia had become the first country in the world to grant regulatory approval to a COVID-19 v...
- WHO awards prequalification to Bharat Bio’s Rotavirus vaccineThe vaccine to prevent infant deaths and hospitalisations due to rotavirus diarrhoea was launched by Prime Minister Narendra Modi in March ...
- Bharat Biotech's typhoid vaccine gets WHO pre-qualificationThis enables the procurement and supplies of this vaccine to UNICEF, Pan-American Health Organisation (PAHO) and GAVI-supported countries, ...
- Cipla Ltd, Strides Arcolab signs collaboration agreements with Medicines for Malaria VentureCipla and Strides will develop a product building on the clinical studies led by TDR, the special programme for research and training in tr...
- Strides gets WHO pre-qualification for anti-malarial tabletsDrug firm Strides Arcolab today said it has received World Health Organisation (WHO) pre- qualification for its anti-malarial tablets.
- Cipla's anti-malaria drug receives WHO pre-qualificationCipla today said an anti-malarial drug developed by Drugs for Neglected Diseases initiative (DNDi) has received pre-qualification from WHO.
- Bharat Biotech to supply Rotavirus vaccine at $ 1Vaccine maker Bharat Biotech will supply India's first indigenously developed diarrhea vaccine to global markets and UN procurement agencie...
- WHO approves Ranbaxy's drug AbacavirPharma major Ranbaxy said the World Health Organisation has approved its anti-retro viral drug Abacavir 300 mg tablets in pre-qualification...
- Ranbaxy gets USFDA nod to market two ARV drugsRanbaxy Laboratories has received US Food and Drug Administration’s (USFDA) approval to manufacture and market two paediatric anti-retrovir...
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