Clinical Trial Database Design
| dc.contributor.author | Divya, S | |
| dc.date.accessioned | 2020-09-24T10:58:43Z | |
| dc.date.available | 2020-09-24T10:58:43Z | |
| dc.date.issued | 2020-09-24T10:58:43Z | |
| dc.description.abstract | CRO specializes in conducting research compared to pharmaceutical companies who themselves are engrossed in a number of other activities like basic R&D, sales and marketing. A contract research organization brings in a lot of value to the pharmaceutical or biotechnology Sponsor Company by reducing costs and also helping to minimize the time period required to conduct the clinical trials. Outsourcing clinical research to CRO helps sponsor companies gather focus on other activities within their organization. Outsourcing helps sponsors convert the fixed costs into variable costs which is being spent on the personnel, expertise and facilities necessary for clinical trial management. If regulations require them to have legal presence in that country to be able to conduct clinical trials or if sponsors do not have complete knowledge of regulatory affairs in a particular country of interest, sponsors may also outsource clinical trials to a CRO. EDC (Electronic Data Capture) is the industry’s leading data engine and the cornerstone of the Medidata Rave, offering fast implementation and maximum control. The flexible architecture lets you collect data across clinical and non-clinical sources and easily integrate with other study capabilities. | en_US |
| dc.identifier.uri | http://hdl.handle.net/123456789/12999 | |
| dc.language.iso | en | en_US |
| dc.subject | Divya S | en_US |
| dc.subject | 1NH18MCA57 | en_US |
| dc.title | Clinical Trial Database Design | en_US |
| dc.type | Other | en_US |