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Showing below up to 50 results in range #951 to #1,000.

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  1. ISO13485 - Clause 1 Scope‏‎ (09:45, 25 August 2020)
  2. ISO13485 - Clause 2 Normative references‏‎ (09:45, 25 August 2020)
  3. ISO13485 - Clause 3 Terms & definitions‏‎ (09:45, 25 August 2020)
  4. Advisory Notice‏‎ (09:45, 25 August 2020)
  5. ISO13485 - 4.1 General Requirements‏‎ (09:45, 25 August 2020)
  6. ISO13485 - 4.2.1 General‏‎ (09:45, 25 August 2020)
  7. ISO13485 - 4.2.2 Quality manual‏‎ (09:45, 25 August 2020)
  8. Quality Manual‏‎ (09:45, 25 August 2020)
  9. ISO13485 - 4.2.3 Control of documents‏‎ (09:45, 25 August 2020)
  10. Record‏‎ (09:45, 25 August 2020)
  11. Document‏‎ (09:45, 25 August 2020)
  12. Legible‏‎ (09:45, 25 August 2020)
  13. ISO13485 - 4.2.4 Control of records‏‎ (09:45, 25 August 2020)
  14. ISO13485 - 5.1 Management commitment‏‎ (09:46, 25 August 2020)
  15. ISO13485 - 5.2 Customer focus‏‎ (09:46, 25 August 2020)
  16. ISO13485 - 5.3 Quality policy‏‎ (09:46, 25 August 2020)
  17. ISO13485 - 5.4.1 Quality objectives‏‎ (09:46, 25 August 2020)
  18. ISO13485 - 5.4.2 Quality management system planning‏‎ (09:46, 25 August 2020)
  19. ISO13485 - Responsibility and authority‏‎ (09:46, 25 August 2020)
  20. ISO13485 - 5.5.2 Management representative‏‎ (09:46, 25 August 2020)
  21. ISO13485 - 5.5.3 Internal communication‏‎ (09:46, 25 August 2020)
  22. ISO13485 - 5.6.1 General‏‎ (09:46, 25 August 2020)
  23. ISO13485 - 5.6.2 Review input‏‎ (09:46, 25 August 2020)
  24. ISO13485 - 5.6.3 Review output‏‎ (09:46, 25 August 2020)
  25. ISO13485 - 6.1 Provision of resources‏‎ (09:46, 25 August 2020)
  26. ISO13485 - 6.2.2 Competence, awareness and training‏‎ (09:46, 25 August 2020)
  27. ISO13485 - 6.2.1 General‏‎ (09:46, 25 August 2020)
  28. ISO13485 - 6.3 Infrastructure‏‎ (09:46, 25 August 2020)
  29. ISO13485 - 6.4 Work environment‏‎ (09:46, 25 August 2020)
  30. ISO13485 - 7.1 Planning of product realization‏‎ (09:46, 25 August 2020)
  31. ISO 14971‏‎ (09:46, 25 August 2020)
  32. ISO13485 - 7.2.1 Determination of requirements related to the product‏‎ (09:46, 25 August 2020)
  33. ISO13485 - 7.2.2 Review of requirements related to the product‏‎ (09:46, 25 August 2020)
  34. ISO13485 - 7.2.3 Customer communication‏‎ (09:46, 25 August 2020)
  35. ISO13485 - 7.3.1 Design and development planning‏‎ (09:46, 25 August 2020)
  36. ISO13485 - 7.3.2 Design and development input‏‎ (09:46, 25 August 2020)
  37. ISO13485 - 7.3.3 Design and development outputs‏‎ (09:46, 25 August 2020)
  38. ISO13485 - 7.3.4 Design and development review‏‎ (09:46, 25 August 2020)
  39. ISO13485 - 7.3.5 Design and development verification‏‎ (09:46, 25 August 2020)
  40. ISO13485 - 7.3.6 Design and development validation‏‎ (09:46, 25 August 2020)
  41. ISO13485 - 7.3.7 Control of design and development changes‏‎ (09:46, 25 August 2020)
  42. ISO13485 - 7.4.1 Purchasing process‏‎ (09:46, 25 August 2020)
  43. ISO13485 - 7.4.2 Purchasing information‏‎ (09:46, 25 August 2020)
  44. ISO13485 - 7.4.3 Verification of purchased product‏‎ (09:46, 25 August 2020)
  45. ISO13485 - 7.5.1.2 Control of production and service provision — Specific requirements‏‎ (09:46, 25 August 2020)
  46. ISO13485 - 7.5.1.3 Particular requirements for sterile medical devices‏‎ (09:46, 25 August 2020)
  47. ISO13485 - Validation of processes for production and service provision‏‎ (09:47, 25 August 2020)
  48. ISO13485 - Control of production and service provisions‏‎ (09:47, 25 August 2020)
  49. ISO13485 - 7.5.3 Identification and traceability‏‎ (09:47, 25 August 2020)
  50. ISO13485 - 7.5.4 Customer property‏‎ (09:47, 25 August 2020)

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