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WPRIM Management System>
DCMS
>
Acta Pharmaceutica Sinica
>
2015
>
50
>
11
Volume:
50
Issue:
11
1. Data quality in clinical trials: the role of blind review.
Page:1498—1501
2. Basic considerations during outsourcing of clinical data management services.
Page:1493—1497
3. Implementation of performance metrics in clinical trial data management.
Page:1488—1492
4. Key issues on the clinical trial data management.
Page:1485—1487
5. Clinical trial data validation and user acceptance testing.
Page:1480—1484
6. Process and method for CDISC-based CRF annotation.
Page:1474—1479
7. Quality control of clinical data management based on EDC.
Page:1470—1473
8. Importance of data management with statistical analysis set division.
Page:1464—1469
9. Comparison of paper and electronic data management in clinical trials.
Page:1461—1463
10. Exploration of visual check approaches in clinical data management.
Page:1456—1460
11. Key factors in design of case report form.
Page:1452—1455
12. Overview of global clinical data management regulations and standards.
Page:1443—1451
13. Global views on clinical trials and data quality.
Page:1434—1442
14. Overview of CDISC standard and implementation in China.
Page:1428—1433
15. Quality control of statistical analysis in data management of clinical trials.
Page:1425—1427
16. Relationship of statistics and data management in clinical trials.
Page:1420—1424
17. The significance, development and prospects of healthcare data integration in new drug clinical trials.
Page:1415—1419
18. Documentation archiving in clinical data management.
Page:1410—1414
19. The importance of clinical data management in improvement of drug evaluation.
Page:1408—1409
20. Prevention and handling of missing data in clinical trials.
Page:1402—1407
21. MedDRA and its applications in statistical analysis of adverse events.
Page:1396—1401
22. Integrated e-clinical solutions in clinical research.
Page:1393—1395
23. Infrastructure and contents of clinical data management plan.
Page:1388—1392
24. Computerized system validation of clinical researches.
Page:1380—1387
25. Clinical trial data management and quality metrics system.
Page:1374—1379
26. Source data management in clinical researches.
Page:1367—1373
27. Master documentation and records in the clinical data management.
Page:1365—1366
28. Master documentation and records in the clinical data management.
Page:1365—6
29. Source data management in clinical researches.
Page:1367—73
30. Clinical trial data management and quality metrics system.
Page:1374—9
31. Computerized system validation of clinical researches.
Page:1380—7
32. Infrastructure and contents of clinical data management plan.
Page:1388—92
33. Integrated e-clinical solutions in clinical research.
Page:1393—5
34. MedDRA and its applications in statistical analysis of adverse events.
Page:1396—401
35. Prevention and handling of missing data in clinical trials.
Page:1402—7
36. The importance of clinical data management in improvement of drug evaluation.
Page:1408—9
37. Documentation archiving in clinical data management.
Page:1410—4
38. The significance, development and prospects of healthcare data integration in new drug clinical trials.
Page:1415—9
39. Relationship of statistics and data management in clinical trials.
Page:1420—4
40. Quality control of statistical analysis in data management of clinical trials.
Page:1425—7
41. Overview of CDISC standard and implementation in China.
Page:1428—33
42. Global views on clinical trials and data quality.
Page:1434—42
43. Overview of global clinical data management regulations and standards.
Page:1443—51
44. Key factors in design of case report form.
Page:1452—5
45. Exploration of visual check approaches in clinical data management.
Page:1456—60
46. Comparison of paper and electronic data management in clinical trials.
Page:1461—3
47. Importance of data management with statistical analysis set division.
Page:1464—9
48. Quality control of clinical data management based on EDC.
Page:1470—3
49. Process and method for CDISC-based CRF annotation.
Page:1474—9
50. Clinical trial data validation and user acceptance testing.
Page:1480—4
51. Key issues on the clinical trial data management.
Page:1485—7
52. Implementation of performance metrics in clinical trial data management.
Page:1488—92
53. Basic considerations during outsourcing of clinical data management services.
Page:1493—7
54. Data quality in clinical trials: the role of blind review.
Page:1498—501
