Merck and Ridgeback seek Emergency Use Authorisation from US FDA for Molnupiravir
If authorised, Molnupiravir could be the first oral anti-viral medicine for the treatment of COVID-19
Sign in
Sign in
Recover your password.
A password will be e-mailed to you.
Browsing Category
Latest Updates
WHO advises additional COVID shot for immunocompromised people
Currently, some 3.5 billion doses of COVID-19 vaccines have been administered, Kate O'Brien, Vaccine Director, WHO, said.
Centre provides over 97 crore COVID-19 vaccine doses to states and UTs
Over 8.22 crore balance and unutilised vaccine doses still available with states and UTs
AstraZeneca launches in-house solar 0.5 MW project as part of ‘Ambition Zero Carbon’
Ambition Zero Carbon sets out to make AstraZeneca’s operations responsible for zero carbon emissions without relying on offset…
IISER Bhopal proposes biochemical link among COVID-19, diabetes and ageing; proposes therapeutic…
The researchers believe that an ideal therapeutic candidate for COVID-19 should be able to target the pathways that are common to…
India currently contributes three-to-five per cent share of the global biotechnology sector
The outsourcing market size for CDMOs in India is roughly at Rs 20,000 crores and it is expected to grow to about Rs 40,000 crores…
Govt allows export of Sputnik Light manufactured in India by Hetero Biopharma
The Russian ambassador had urged the Indian government to allow the export of Sputnik Light produced by Hetero Biopharma, one of…
NMPB and IHBT sign MoU to produce planting material for medicinal plants
NMPB works towards supporting policies and programmes for the growth of trade, export, conservation and cultivation of medicinal…
US FDA grants breakthrough therapy designation to Roche’s anti-amyloid beta antibody gantenerumab
Gantenerumab is an investigational antibody in phase-III development for early Alzheimer's disease (AD)
WHO says ‘near’ to solving issues on Russia’s Sputnik V vaccine
Russian Health Minister Mikhail Murashko said last week that all barriers to register the vaccine with the WHO had been cleared…
Zydus Cadila receives tentative approval from US FDA for Adapalene and Benzoyl Peroxide Gel
The product works by killing the bacteria that cause acne and by keeping the skin pores clean
Australian regulator approves Lincoln Pharmaceuticals’ Gujarat plant for GMP
TGA and EU GMP approval will strengthen the company's presence in the regulated markets
Bharat Biotech submits clinical trial data of Covaxin in children to CDSCO
As part of the phase-II/III trial, the two-dose Covaxin was administered with 28 days apart.
Simulation technology for pharma and biopharma
Rafiq Somani, Area Vice President – India and South Asia Pacific, Ansys, explains why simulation technology is a win-win for…
India is the fastest growing market across the globe for Waters
Dr Udit Batra, CEO and President, Waters Corporation reviews his company's strategy to cope with the pandemic, and bounce back to…
Docmode breaks COVID-induced barrier with Gapsule
The novel initiative is expected to bridge the COVID-induced knowledge and relationship gap between physicians and pharma…
Second inter-ministerial meeting between health and AYUSH ministries generates momentum
Ministers show resolve to achieve effective coordination; officials discussed the nuances of cooperation strategies
Researchers from Germany and US receive Nobel Prize in Chemistry 2021
The Nobel Prize for 2021 was awarded jointly to Benjamin List and David WC MacMillan for the development of asymmetric…
Sustainability in Pharma– Leapfrogging into a Carbon Neutral World
Express Pharma, in association with SAP India, as part of the Life Sciences Industry Knowledge Exchange Forum, recently hosted a…
Pharmapack Report 2021: Digital data democratisation, environmental factors and user experience…
Ocular delivery and interactive packaging forecast to see big developments