Quality Systems:in Pharmaceutical Industry

Here are some catchy phrase lines for various ISO systems and quality audit systems in the pharma industry:

1. *ISO 9001*: "Quality that Prescribes Excellence"

2. *ISO 13485*: "Medicine Meets Management Mastery"

3. *GMP*: "Good Manufacturing Practices for a Healthy Reputation"

4. *GDP*: "Good Distribution Practices for a Secure Supply Chain"

5. *GLP*: "Good Laboratory Practices for Reliable Results"

6. *ISO 17025*: "Testing the Limits of Quality"

7. *ISO 14001*: "Sustainable Practices for a Greener Pharma"

8. *OHSAS 18001*: "Safety First in Every Prescription"

9. *ISO 22000*: "Food for Thought, Quality for Life"

10. *FSSC 22000*: "Feeding Safe Solutions to the Pharma Industry"

For quality audit systems:

1. *Internal Audits*: "Checking the Pulse of Quality"

2. *External Audits*: "Third-Party Validation for Peace of Mind"

3. *Supplier Audits*: "Ensuring Quality from Source to Shelf"

4. *Regulatory Audits*: "Compliance that Cures"

The pharmaceutical industry uses various ISO systems and quality audit systems to ensure compliance with regulatory requirements and industry standards. Here are some of the most common ones:

ISO Systems:

1. *ISO 9001*: Quality Management System (QMS) standard for overall quality management.

2. *ISO 13485*: Medical Devices - Quality Management Systems - Requirements for Regulatory Purposes.

3. *ISO 14001*: Environmental Management System (EMS) standard for environmental management.

4. *ISO 22000*: Food Safety Management System (FSMS) standard for food safety.

5. *ISO 45001*: Occupational Health and Safety Management System (OHSMS) standard for occupational health and safety.

Quality Audit Systems:

1. *GMP (Good Manufacturing Practice)*: Audits for compliance with GMP regulations.

2. *GDP (Good Distribution Practice)*: Audits for compliance with GDP regulations.

3. *GLP (Good Laboratory Practice)*: Audits for compliance with GLP regulations.

4. *GCP (Good Clinical Practice)*: Audits for compliance with GCP regulations.

5. *ISO 19011*: Guidelines for auditing management systems.

6. *PDA (Parenteral Drug Association)*: Audits for compliance with PDA standards.

7. *PIC/S (Pharmaceutical Inspection Convention/Pharmaceutical Inspection Scheme)*: Audits for compliance with PIC/S standards.

Other Quality Systems:

1. *Six Sigma*: A data-driven approach to quality management.

2. *Lean*: A methodology for eliminating waste and improving efficiency.

3. *Total Quality Management (TQM)*: A holistic approach to quality management.

4. *Continuous Quality Improvement (CQI)*: A systematic approach to quality improvement.

Regulatory Audits:

1. *FDA (Food and Drug Administration)*: Audits for compliance with FDA regulations.

2. *EMA (European Medicines Agency)*: Audits for compliance with EMA regulations.

3. *WHO (World Health Organization)*: Audits for compliance with WHO regulations.

Note that this is not an exhaustive list, and the specific ISO systems and quality audit systems used may vary depending on the country, region, or industry segment.

Let me know if you'd like me to come up with more options or if you have any specific preferences!