Disruptive forces made Clinical Research Organisations(CROs) looking at all options to boost growth and competitiveness. In one hand CRO industry under tremendous pressure to constantly increase efficiency and drive innovation in their operations on the other hand many Pharma companies…
Fourth Successful Vendor Audit of Global Regulatory & Consumer Insights (GR-CIS)
This is a testimony that GR-CIS is one among few Regulatory Service provider in the country who not only believes in QUALITY but excel in the same. With no findings and no observations this was the fourth audit in a…
India to unveil new drug policy: officials
India is expected to roll out a new drug policy and devise rules for clinical trials that may bring new projects to the country, a top Indian official have said. A team of Indian officials led by G N Singh,…
Google Offshoot Starts A 10,000-Person Study To Plumb Human Biology
It’s a realistic blueprint for how tech could change medicine. But it’s also an emblem of how long that transformation will take. Verily, formerly known as Google Life Sciences, plans to begin a long-awaited 10,000-person study to explore the biology of healthy people in…
FDA in India – Championing a Culture of Quality
One of FDA’s most strategic outposts is in India, the seventh largest supplier of food and second largest supplier of pharmaceuticals and biologics to the United States. The agency’s office, located in the capital, New Delhi, works to ensure the…
Report: Global drug market will hit $1.5T in 2021
Total spending on medicines is forecast to reach $1.5 trillion by 2021, up 33% from 2016 levels, even as annual growth moderates from the record pace set in 2014 and 2015, according to new research released by the QuintilesIMS Institute. While…
CDSCO has issued another circular which indicates that CDSCO is making Rules and Regulations more Industry Friendly
CDSCO has issued circular dated 03 Aug 2016 regarding “Requirement of NOC from DCGI for addition of new clinical trial site or investigator”wherein they have stated that just notification of addition of site/investigator to DCGI is required. However the respective…
