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| AGES PharmMed – April 2012 |
| Successful inspection of a Bioequivalence study and Quality Management System of FCRL by AGES PharmMed – Austrian Agency for Health and Food Safety and BASG – Austrian Federal Office for Safety in Health Care” done in April 2012. |
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| USFDA - July 2010, June 2011 and October 2011 |
| Our studies have been inspected and approved by USFDA. |
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| afssaps (France) February 2008 |
| The FCRL facility has been inspected by the French Regulatory Authority, afssaps. It underwent a successful audit for two studies submitted to France and Denmark. The inspection covered all aspects of the study related activities- besides facility & quality systems audit. |
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| ANVISA (Brazil) March 2006, August 2007, August 2009 and February 2012 |
| Approved as a GCP-compliant site for clinical, bioanalytical and statistical support for BA/BE studies. |
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| DCGI (India) January 2006 |
| Approved by Drugs Controller General of India (DCGI) to conduct clinical studies with the new Drugs. |
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| DSIR (India) |
| Approved as a research centre by Department of Scientific and Industrial Research (DSIR), Govt. of India. |
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