Gujarat launches a web portal for cosmetics licensing EP News Bureau Dec 26, 2022 Through this web portal, the recognised manufacturers in the state will be able to do all work related to licensing and…
Sun Pharma gets Form 483 from US FDA for regulatory violations at Halol plant Press Trust of India May 11, 2022 The US Food and Drug Administration (FDA) conducted a Good Manufacturing Practices (GMP) inspection of the Halol facility from…
16 pharma units get ‘stop production orders’ for norm violations from Maha FDA Press Trust of India Apr 13, 2022 It comes after the regulator carried out inspection of 655 pharma manufacturing facilities in the last three months in the state
WHO establishes global biomanufacturing training hub in Republic of Korea EP News Bureau Feb 24, 2022 Bangladesh, Indonesia, Pakistan, Serbia and Vietnam to receive mRNA technology from the technology transfer hub
OPPI-QCI announce Quality Award for Excellent Facility of the year, 2021 EP News Bureau Feb 10, 2022 The Award is instituted by OPPI in collaboration with QCI to recognise pharmaceutical facilities excelling in quality…
Sputnik V due to submit vaccine data to WHO this month Reuters Dec 22, 2021 Moscow rushed to approve the shot for domestic use last year and it has been exported to countries around the world, but it has…
Piyush Goyal asks pharma industry to strive for quality, absorb global experiences Usha Sharma Feb 26, 2021 He said that we can provide the world with the confidence that if there is anything to do with health, then India is the place to…
Drugs & Cosmetics Act, 1940: Recommendations for a revamp Usha Sharma Nov 20, 2020 The existing Drugs and Cosmetics Act of 1940 was formed during the pre-independence era. Since then, amendments have been made to…
Quality: How serious are we? EP News Bureau Aug 23, 2020 Alok Ghosh, Ex-President - Global Technical Operations, Lupin, informs that with increasing competition and price control, it is…
VAV Lipids gets written confirmation from CDSCO for Ratnagiri facility EP News Bureau Aug 10, 2020 This confirmation is a requisite to import active substances into the EU for medicinal products of human use