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:
- Procedure For Preparation, Control, Distribution, Issuance, Retrieval And Archiving Of Standard Operating Procedures (Sop On Sop)
- Format Issuance & Control
- Traning Management Procedure
- Change Control Management Procedure
- Capa Management Procedure
- Numbering Procedure For Equipment/Instruments
- Specimen Signature
- Good Documentation Practices
- Vendor Qualification
- Sop For Validation Life Cycle
- Preparation Of Validation Master Plan
- Job Description
- Receipt, Storage, Issuance, Retrieval, Retention And Destruction Of Documents
- Management Of Data Intigrity
- Deviation Management
- Investigation Management
- Quality Risk Managment
- Annual Product Quality Review
- Self Inspection
- Process Validation
- handling Of Product Recall
- Handling Of Product Recall
- line Clerance
- technology Transfer
- managment Review Meetings
- cleaning Validation
- Computer System Validation
- Procedure For Preparation Of Site Master File
- Out Of Specificaton
- Handling Of Event/Incident
- Quality Manual
- URS
- determination Of Significant Figures And Rounding Values
- Investigation In Pharmaceuticals
- Oos And Oot
- Total Quality Management System (Tqm)
- quality Metrics For Pharmacutical Manufacturing
- alcoa And Alcoa Plus In Data Integrity
- Importance Of Six Sigma In Pharmaceutical Industry
- Qualification of compressed air.
- Fat And Sat
- Types Of Water In Pharmaceutical Industry
- Vacum Leak Test
- Role Of Quality Assurance
- Transport Validation
- Gowning Qualification
- Data Integrity
- APQR
- Difference Between Validation, Calibration And Qualification
- Procedure For Line Clearance