Webinar - The new QMS Normal Post COVID19 for the Pharma, Life Sciences & Medical Device Companies



FDA, EMEA and Now Indian regulatory authorities have made it mandatory to conduct clinical trial inspections for all the trials. With the latest development, not only sites, but sponsors and CROs also have a high possibility of getting inspected. For you to handle inspections successfully, we are there to assist you. We shall make your site ready to face inspection, handle findings and respond to the same in the best possible efficient manner or CRQA can act on your behalf and answer all queries coming from RA.

For System Demo and further information, please call +91 98100 68241 or mail us at bd@crqa.in