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Engaging with authorities to address challenges regarding manufacturing, distribution of drugs: OPPI
OPPI continues to remain engaged with the relevant authorities to ensure that these challenges are overcome at the earliest, he…
DGFT bans export of hydroxychloroquine from SEZs, EOUs too
ICMR) recommended the use of hydroxychloroquine for prophylaxis to asymptomatic healthcare workers involved in the care of…
DoP seeks MHA intervention for uninterrupted pharma ancillary supplies
Due to nationwide lockdown because of Coronavirus (Covid-19), apart from challenges in transportation and availability of…
Thermo Fisher Scientific to enhance capacity for COVID-19 testing in India
The company has has received Emergency Use Authorization (EUA) by the US Food and Drug Administration for its TaqPathCOVID-19…
Lupin’s Aurangabad Facility Receives EIR from US FDA
The inspection for the facility was carried out between February 10, 2020 and February 14, 2020 and concluded with no observations
Passenger aircrafts now allowed to transport pharma exports: DGCA
The development is a welcome measure as restrictions on exports coupled with the logistic issues have put exporters in a…
DSM completes acquisition of Human Milk Oligosaccharides supplier, Glycom
There is significant interest in HMO use as a dietary supplement and potentially in food and beverage and pet food applications,…
Central Board of Narcotics allows scan copy application and considers routine permits for…
Once the lockdown is lifted by the Union Government, the exporter/importer of narcotic drugs/Psychotropic Substances and…
US FDA calls for removal of all ranitidine products
New studies show NDMA impurity increases in some meds over time, and when stored at higher than room temperature
Agilent Cary UV Workstation Software for Cary 3500
US FDA Part 11 in Title 21 of the Code of Federal Regulations (CFR), and its EU analog, Eudralex Chapter 4, Annex 11, describe the…