BioVoice News July 2017 Issue 2 Volume 2 | Page 59

“In that regard, we would now like to inform you that we have received an establishment inspection report (EIR) from the USFDA as the closure of audit for the above- referred facility,” the drug maker said its filing. INDIAN R&D EFFORTS INTO HEALTH & ENVIRONMENT ALL SET TO GET A NEW BOOST Research and development efforts in the areas of health and environment are set to get a major boost with the Government of India becoming an Associate Member of European Union’s cutting edge Synchrotron Radiation Facility (ESRF) at Grenoble in France. The agreement will be for a period of three years at a cost of Rs 17.5 crore. It will provide Indian scientific community access to multiple beam lines and other cutting edge facilities. India is the 22nd country to join the Facility. The agreement builds up on the success of a previous ad- hoc arrangement signed by the Department of Biotechnology (DBT) with European Molecular Biology Laboratory (EMBL) in 2008 to access a beam line called BM14 at the Facility. The project was implemented by the New Delhi based National Institute of Immunology (NII) in partnership with EMBL. Under the new arrangement, that was formally launched in the presence of the Minister for Science and Technology, Harsh Vardhan on June 19, India became a scientific partner of ESRF through the Regional Centre for Biotechnology (RCB), Faridabad. three observations. ASTRAZENECA GETS DCGI’S APPROVAL FOR ASTHMA DRUG, SYMBICORT 320 AstraZeneca Pharma India Limited (AstraZeneca India), a leading global biopharmaceutical company has received marketing authorisation from the Drug Controller General of India (DCGI) for Symbicort 320 mcg. The drug a fixed-dose combination comprising budesonide and formoterol BIOVOICENEWS.COM 59