Pages without language links

Jump to: navigation, search

The following pages do not link to other language versions.

Showing below up to 50 results in range #31 to #80.

View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)

  1. 1.5.2.4 Principal investigators and study directors
  2. 1.5.2.5 Research team
  3. 1.5.2.6 Supporting team
  4. 1.5.2.7 Quality professionals
  5. 1.5.2 Roles and responsibilities of involved personnel and organization
  6. 1.5.3.1 Personnel
  7. 1.5.3.2 Facilities
  8. 1.5.3.3 Laboratory and experimental equipment used for measurement
  9. 1.5.3.4 Electronic information system
  10. 1.5.3.5 Organization-specific know how
  11. 1.5.3.6 Documentation requirement for sample and material
  12. 1.5.3.7 Retained personnel records
  13. 1.5.3 Management of resources
  14. 1.5.4.1 Independence of internal compliance assessment
  15. 1.5.4.2 Internal assessment of the organizations' quality professionals
  16. 1.5.4 Prevention of Conflict of Interest
  17. 1.5.5 Sustainability
  18. 2.1.10 Plausibility check
  19. 2.1.11 Preregistration
  20. 2.1.1 Study protocol
  21. 2.1.2 Unique study ID
  22. 2.1.3 Appraisal of literature and systematic reviews
  23. 2.1.4 Purpose of research
  24. 2.1.5 Pre-specification
  25. 2.1.6 Sample size and power analysis
  26. 2.1.7 Blinding
  27. 2.1.8 Randomisation
  28. 2.1.9 Inclusion and exclusion criteria
  29. 2.2.1 Use of SOPs for standard experiments
  30. 2.2.2 Use of template for (manual) data recording
  31. 2.2.3 Documentation of the experiment and deviations
  32. 2.3.1.1 Converting non-electronic information into an electronic form
  33. 2.3.1 Generation, recording, handling and archiving of raw data
  34. 2.3.2 Primary analysis and evaluation of raw data
  35. 2.3.3 Statistical analysis
  36. 2.3.4 Data visualization
  37. 2.4.1 Non-public reporting
  38. 2.4.2 Publication
  39. 2.4 Reporting
  40. 3.1.1 Platform to record data
  41. 3.1.2.1 Traceability of data and any person having impact on data
  42. 3.1.2.1 Traceability of data and any person having impact on data​
  43. 3.1.2.2 Process for witnessing of records
  44. 3.1.2 Procedures for how and when to record data
  45. 3.1.3 Data security
  46. 3.2.1 General guidance on training
  47. 3.2.2 Good Research Practice training
  48. 3.2.3 Implementation of the EQIPD Quality System
  49. 3.2.4 Training on specific methods, tasks and activities
  50. 3.3.1 Fit-for-purpose working environment

View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)