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Friday, July 12, 2019
8:00 AM - 2:00 PM
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http://www.globalcompliancepanel.com/virtual-seminar/6-hour-virtual-seminar-on-clinical-data-management---part-ii--10203LIVE?upcomingevents-Jul-SEO-20
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When new drugs or devices are tested in humans, the data generated by, and related to, these trials are known as clinical data. This data represents a huge investment by the biopharmaceutical or device company and is one of its greatest assets. It is this data that will eventually make a new product both useful as a treatment or therapy and marketable.
The management of clinical data, from its collection during a trial to its extraction for analysis, has become a critical element in the steps to prepare a regulatory submission and to obtain approval to market a treatment.
The management of clinical data, from its collection during a trial to its extraction for analysis, has become a critical element in the steps to prepare a regulatory submission and to obtain approval to market a treatment.