QA

Quality assurance comprises administrative and procedural activities implemented in a quality system so that requirements and goals for a product, service or activity will be fulfilled. It is the systematic measurement, comparison with a standard, monitoring of processes and an associated feedback loop that confers error prevention. This can be contrasted with quality control, which is focused on process output.
The terms “quality assurance” and “quality control” are often used interchangeably to refer to ways of ensuring the quality of a service or product. For instance, the term “assurance” is often used for Implementation of inspection and structured testing. The term “control”, however, is used to describe the fifth phase of the Define, Measure, Analyze, Improve, Control (DMAIC) model. DMAIC is a data-driven quality strategy used to improve processes.
Quality assurance includes two principles: “Fit for purpose” (the product should be suitable for the intended purpose); and “right first time” (mistakes should be eliminated). QA includes management of the quality of raw materials, assemblies, products and components, services related to production, and management, production and inspection processes.
Quality assurance is a wide ranging concept covering all matters that individually or collectively influence the quality of a product.

The following are some of the procedures of quality assurance  to be followed:

  1. Procedure For Preparation, Control, Distribution, Issuance, Retrieval And Archiving Of Standard Operating Procedures (Sop On Sop)
  2. Format Issuance & Control
  3. Traning Management Procedure
  4. Change Control Management Procedure
  5. Capa Management Procedure
  6. Numbering Procedure For Equipment/Instruments
  7. Specimen Signature
  8. Good Documentation Practices
  9. Vendor Qualification
  10. Sop For Validation Life Cycle
  11. Preparation Of Validation Master Plan
  12. Job Description
  13. Receipt, Storage, Issuance, Retrieval, Retention And Destruction Of Documents
  14. Management Of Data Intigrity
  15. Deviation Management
  16. Investigation Management
  17. Quality Risk Managment
  18. Annual Product Quality Review
  19. Self Inspection
  20. Process Validation
  21. handling Of Product Recall
  22. Handling Of Product Recall
  23. line Clerance
  24. technology Transfer
  25. managment Review Meetings
  26. cleaning Validation
  27. Computer System Validation
  28. Procedure For Preparation Of Site Master File
  29. Out Of Specificaton
  30. Handling Of Event/Incident
  31. Quality Manual
  32. URS
  33. determination Of Significant Figures And Rounding Values
  34. Investigation In Pharmaceuticals
  35. Oos And Oot
  36. Total Quality Management System (Tqm)
  37. quality Metrics For Pharmacutical Manufacturing
  38. alcoa And Alcoa Plus In Data Integrity
  39. Importance Of Six Sigma In Pharmaceutical Industry
  40. Qualification of compressed air.
  41. Fat And Sat
  42. Types Of Water In Pharmaceutical Industry
  43. Vacum Leak Test
  44. Role Of Quality Assurance
  45. Transport Validation
  46. Gowning Qualification
  47. Data Integrity
  48. APQR
  49. Difference Between Validation, Calibration And Qualification
  50. Procedure For Line Clearance